Search results “Pharmaceutical product manufacturing process”
Phases of Pharmaceutical Industry
The video-clip 'Phases of pharmaceutical industry' presents, step by step, the medicine line production. A 2D animation presents both the individual phases and the overall picture of the process. The students familiarize with the requirements and the conditions of medicine production, the required technology and the importance of health and safety specifications. What follows is the acquaintance with the methods of product qualitative control, the role of the head pf production and issues of waste management. The clip is instructional as far as medicine production is concerned and can be used as an introduction to the topic 'Industries' and 'Pharmacy'.
Views: 188973 EducationalTVGreece
Advanced Pharmaceutical Manufacturing
There are a number of challenges that the industry faces in order to transition towards more competitive, systematic and efficient manufacturing. Regulatory authorities have recognized the deficiencies of pharmaceutical product manufacturing and aim to enhance process understanding through Quality by Design (QbD) and Process Analytical Technology (PAT) tools. As a result of this current effort to change the mindset in order to mimic the rest of the chemical industry, an additional transition is becoming more and more appealing: transition from batch to continuous production mode. However, continuous manufacturing requires detailed process understanding in terms of the evolution of all critical material properties as a function of its operating parameters and environmental conditions. Once process knowledge is translated into models, computer aided dynamic simulation tools will allow the design, analysis and optimization of continuous integrated processes. In this talk I will discuss the work that has been done in my lab towards the development of an integrated platform that will enable the efficient flowsheet simulation and analysis, the assessment of design alternatives, the feasibility analysis of the production line, and the control and optimization of process design and operations. The developed flowsheet model includes modules for all the necessary unit operations, namely powder feeding, mixing, roller compaction, tablet press and milling integrated to represent a tablet manufacturing line. Models used to represent each unit operation vary from empirical, first-principle or hybrid. Population balance models are developed in order to track the composition and particle size changes throughout complex powder processes dynamically. The developed flowsheet simulation is used to predict the propagation of upstream disturbances to final product quality, the assessment of recycle stream benefits, the identification of process integration bottlenecks and evaluation of different control strategies in order to retain the process within its design space. In addition, global dynamic sensitivity analysis is performed to identify critical process parameters not only within each unit operation, but also between different processes. Finally, simulation based optimization techniques enable the identification of the optimal operating conditions, as well as the optimal design sequence which leads to pharmaceutical tablets with desired characteristics. This work aims to merge knowledge, experience, experimental results and modeling tools for developing a dynamic simulation platform that will enable the safe implementation of the transition towards continuous pharmaceutical manufacturing. Biography: Marianthi Ierapetritou is a Professor and Chair in the Department of Chemical and Biochemical Engineering at Rutgers University in Piscataway, New Jersey. Dr. Ierapetritou’s research focuses on the following areas: 1) process operations; (2) design and synthesis of flexible production systems focusing on pharmaceutical manufacturing; 3) modeling of reactive flow processes; and 4) metabolic engineering with focus on biopharmaceutical production. Her research is supported by several federal (NIH, NSF, ONR, NASA) and industrial (BMS, J&J, ExxonMobil, Honeywell, Cardinal Health) grants. Among her accomplishments are the Outstanding Faculty Award, the Rutgers Board of Trustees Research Fellowship for Scholarly Excellence, and the prestigious NSF CAREER award. She has more than 180 publications, and has been an invited speaker to numerous national and international conferences. Dr. Ierapetritou obtained her BS from The National Technical University in Athens, Greece, her PhD from Imperial College (London, UK) in 1995 and subsequently completed her post-doctoral research at Princeton University (Princeton, NJ) before joining Rutgers University in 1998.
Views: 41754 APMonitor.com
Sterile pharmaceutical manufacturing process plant
Sterile pharmaceutical manufacturing # Plant operation https://hvacelectricalinterviewtips.b... https://www.facebook.com/andrewtechvi... http://cogismith.com/1csx
Development and Delivery of Pharmaceutical Products  (CMC) - MaRS Best Practices
Moving from drug discovery to drug development requires a particular skillset usually not yet honed by start-ups. This phase of the development process is highly regulated and critical. Let Dr. Colin Minchom take you through the aspects of the Chemistry, Manufacturing and Control (CMC) portion of the drug development process. Watch this video to learn about the pharmaceutical product development which includes objectives of formulation, cost-effective strategies to reach key milestones and more. MaRS -- Building Canada's next generation of global technology companies. marsdd.com
Theon Pharmaceuticals Ltd, Baddi-Best Third Party Contract Manufacturing Pharmaceutical formulations
Theon Pharmaceuticals Ltd Since its inception in 2005, Theon Pharmaceuticals Ltd., a WHO-GMP & ISO 9001:2008 certified company is a rapidly growing professionally managed Indian Pharmaceutical Company and is now effectively harnessing global opportunities to fortify its international presence. Theon’s State of the art modern facilities are spread over 4.5 Acres, located in lush green, excise free zone of Nalagarh in the state of Himachal Pradesh. This excise free zone is a hub of leading pharmaceutical companies of India as it provides a cost competitive edge over manufacturing units operating in other parts of India. The Company boasts of an impressive product list inclusive of niche DCGI approved formulations to meet all customer needs. It is presently a co-producer to leading pharmaceutical companies of India. • WHO - GMP and ISO 9001:2008 Certified Company • Leading Contract Manufacturing Company in the Country • State of the art Infrastructure • Dedicated and Fabricated Blocks for General, Betalactam & Cephalosporins • Automated Machines & High - Speed packing lines • Dedicated Modular Labs complying GLP norms • 100% Excise Free Zone • Exporting to ASIAN, AFRICAN & CIS Countries • NABL accredited Modular laboratories with latest sophisticated instruments Including UPLCs Theon has marked its presence globally by exporting its products to Africa, Central Asia, CIS, French West Africa, Latin America and South East Asia. We have an array of Certification. • WHO-GMP • PPB - Kenya • NDA - Uganda • FMHACA - Ethiopia • TFDA - Tanzania • MOH - Vietnam • DPM - Ivory Coast • MOH - Sri Lanka • MOH – Afghanistan • FDA- Philippines • GMP • Neutral Code (for exports) • Dietary Supplement License • Non - Conviction Certificate • ISO 9001: 2008 • NSIC - CRISIL Rating: SE 1A & BBB+ The Company has dedicated & segregated blocks for General, Penicillins (ß-lactam) & Cephalosporins dosages in the form of Tablets, Capsules, Ointments, Sachets, Injectables and Dry Syrups covering all major therapeutic segments. To carry out Real Time & Accelerated Stability Studies as per ICH guidelines, the Company maintains separate dedicated R&D laboratories and stability chambers & laboratories. For strict compliance of Good Laboratories Practices (GLP's), the Company has latest sophisticated instruments in its in-house chemical, instrumental & microbiological laboratories. Theon aims at carving a place for itself in the Indian Pharmaceutical market with specialization in new and niche molecules thereby adding value for their clients as well as customers. Theon's Global Presence Streamlining the export vision at Theon, a dedicated Export regulatory department team has been set up for complying with international audits and providing complete export documentation including COPP and dossier preparations as per CTD format. Operating in total compliance with c-GMP norms, Theon's manufacturing unit has been granted certifications by PPB - Kenya, NDA - Uganda, FMHACA - Ethiopia, TFDA - Tanzania, MOH - Vietnam, DPM - Ivory Coast, MoH - Sri Lanka, MOH - Afghanistan and several others in pipeline. Theon is currently catering to Africa, South East Asia, Central Asia, French West Africa, CIS, Latin America, Asia Pacific and many more and we endeavour to become the world class pharmaceutical manufacturer for India & neighboring countries and to assist in the development of quality products by providing superior performance with high class products in right budget. Salient Features • Built up area of 1,75,000 sq. ft with separate areas for production and stores • Quality Control, HVAC, Utilities and Administration • Separate entry and exit for man, material & service personnel for both • Designed and built as per vertical flow concept of man – material movement • c-GMP compliant latest manufacturing equipments • NABL accredited Modular laboratories with latest sophisticated instruments Including UPLCs • Highly skilled, dedicated and experienced technical staff • Automated access control system and fully equipped cameras • Immaculate environmental monitoring, calibration and validation programme Quality & innovation are the hallmark of Theon. At Theon, we strongly support Environmentalism, and keeping in mind the same, we use innovative method & technology to have highest standards of Safety, Environment and Health in our manufacturing processes. A passion for innovation…. A commitment to excellence…. A reputation for reliability…. THEON PHARMACEUTICALS LTD. For healthy lives……..
Views: 95801 Naveen Thakur
कैसे करे मेडिसिन की मैन्युफैक्चरिंग यूनिट शुरू How to start Pharmaceutical Manufacturing Unit
If you want to set-up a plant or manufacturing unit in Pharmaceutical Sector, then this video will help you to understand complete information, licenses required, procedure, documents, minimum area required section wise and individually. This video will help you to understand process for getting manufacturing unit licence in pharmaceutical sector. More detail with list of machinery and equipment read at following link: https://pharmafranchisehelp.com/2016/02/how-to-start-pharmaceutical-cosmetic-manufacturing-unit.html
Views: 6318 Pharma Franchise Help
Pharmaceutical Product Lifecycle Management
The presentation gives details of Production Life Cycle begining from lab to final launch, applicable in pharmaceutical and Biopharmaceutical industry.
Views: 3384 Biobridge Healthcare
Biotech production at Roche in Basel: find out more
Only a few decades ago, the idea of harnessing biotechnology to produce medicines appeared highly fanciful. Why? Unlike conventional drug ingredients produced by purely chemical methods, biotechnologically produced medicines are much more complex and difficult to manufacture. Today, these drugs have become must-haves for the treatment of several serious diseases. Biotechnologically produced treatment tools are now available for several diseases (cancer in particular), providing a beacon of hope for thousands of patients. Roche is No. 1 in the world in biotechnology. With its research, development and production sites across the globe, Roche offers doctors and patients alike a vast range of biopharmaceuticals and diagnostic tests manufactured using biotechnology. One biotechnology production site, located at our headquarters in Basel, is showcased in this video. To further explore the life science cluster in Basel visit: https://www.roche.com/research_and_de... Subscribe to our YouTube channel now: https://www.youtube.com/user/roche?sub_confirmation=1 Get in touch with us: https://www.roche.com/ https://www.facebook.com/RocheCareers https://www.linkedin.com/company/roche https://twitter.com/roche Roche has been committed to improving lives since the company was founded in 1896 in Basel, Switzerland. Today, Roche creates innovative medicines and diagnostic tests that help millions of patients globally. Roche is a leader in research-focused healthcare with combined strengths in pharmaceuticals and diagnostics. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and neuroscience. For more information and insights visit: https://www.roche.com/
Views: 55106 Roche
Bioprocessing Part 1: Fermentation
This video describes the role of the fermentation process in the creation of biological products and illustrates commercial-scale fermentation at a cellular level. Included are descriptions of types of fermentation (intracellular, extracellular), types of cells (aerobic, anaerobic), and cell nutrition (media components). The program follows the production of a batch of Green Fluorescent Protein (GFP) from preparation through harvesting, including growth of seed stock, scaling up, and life cycle growth pattern phases (lag, exponential/log, stationary, death). Featured throughout is the monitoring of various production process parameters, including time, temperature, pressure, pH, agitation, etc. For free eLearning resources, check out http://www.ncbionetwork.org/educational-resources/elearning.
Views: 235186 BioNetwork
Manufacturing Drugs at Large Scale
Discover how Biogen Idec's industry-recognized expertise in manufacturing biologic therapies blends a combination of innovation and collaboration to ensure quality and reliable drugs.
Views: 40160 Biogen
Pharmaceutical Continuous Manufacturing Technology and Applications
USP is exploring how its extensive expertise in developing quality standards for drug products and ingredients can contribute to pharmaceutical continuous manufacturing
Views: 3940 US Pharmacopeia
Oral Liquid Syrup Filling line ,Oral Liquid Production Line
E-mail : [email protected] or Call Now : + 91 9898070475 Oral Liquid Filling Line, Liquid Syrup Filling line ,Oral Liquid Production Line call + 91 9898070475 or visit http://www.bhagwatipharma.co.in Watch our machinery videos : http://www.bhagwatipharma.co.in As an incorporated body of washing, drying and filling, this oral liquid production line is specially designed for washing, drying, filling, capping and sealing 10ml or 500ml linear glass bottles, PET with easy open lids. The main components of it are double screw bottle washing dryer and the filling capping labeling device Oral Liquid Filling Line, Liquid Syrup Filling line ,Oral Liquid Production Line -USA, France, Poland, Bulgaria, Saudi Arabia, Ecuador, Peru, South Africa, Egypt, Indonesia, UAE, Vietnam, Pakistan, Uganda, Philippines, Greece, Columbia, Malaysia, Nigeria, Ethiopia, Lebanon, Kenya, Kuwait, Sri Lanka, Ghana, Nepal, Ukraine, Bangladesh, Australia, Switzerland, Sudan, Russia, Yemen, Iran, Morocco, Malawi, Thailand, Tanzania, Canada, Belarus ,USA ,Cyprus ,UAE ,Republic of Congo ,Canada ,Russia ,South Africa ,Crotia ,Nepal ,OMAN ,UKRAINE ,China ,Bhutan ,Ghana ,Yugoslavia ,Nigeria ,Netherlands ,Vietnam ,Thailand ,Kenya ,Iran ,Malaysia ,Bangladesh ,Pakistan, U.A.E , SAUDI ARABIA , Monrovia , Phillipines , Spain ,Liberia , Iran ,U.S.A, Canada, Germany, Italy, Jordan, Syria, Turkey, Kuwait, Iran, Algeria, Argentina, Bangladesh, Bangkok, Indonesia, Malaysia, Vietnam, Nigeria, Ghana, Malawi, Egypt, Ukraine, Nepal, Srilanka, Bangladesh, Tibet Lusaka, Egypt, England, UAE, Bahrain, Vietnam, Iran, Poland, Tanzania, Malaysia, Nigeria, Sudan, U.K., Italy, Thailand, Span, Kenya, Lebanon, Kingdom of Saudi Arabia, Sudan, Botswana, Iraq, Thailand, Span, Mauritius, Ethopia, Congo, Zambia, Namibia, Mozambique, Uganda, Yemen, Somaliya, Oman, Jordan, Turkey, Labia, Morocco, France, Germany, Ukraine, Turkey, Greece, Kazakhstan, Russia, Uzbekistan, Malaysia, Thailand,Singapore, Philipines, Indonesia, Australlia, New Zealand etc.For more product our group please refer below video http://www.powderfillingmachine.net/ http://www.liquidmanufacturingplant.com/ http://www.liquidmixingplant.com/ http://www.tubefillingmachine.net/ http://www.liquidfillingmachines.net/ http://www.capsealingmachine.net/ http://www.ointmentplant.net/ http://www.toothpasteplant.com/ http://www.blenderindia.net/ http://www.vibrosifter.net/ http://www.liquidbottlingplant.com/ http://www.storagetankindia.com/ http://www.filterpressindia.net/ http://www.labelingmachineindia.net/ http://www.bottlewashingmachine.net/
Achieve Quality Initiatives Throughout the Pharmaceutical Manufacturing Process | Thermo Scientific
Learn more at www.thermoscientific.com/rmid. For global pharmaceutical industry -- From raw material verification to chemical dispensing and secondary operations through to finished product inspection, Thermo Scientific TruScan and microPHAZIR handheld analyzers provide manufacturers with a portable analytical instrument solution to achieve quality standards at the point of need.
Medicine Capsule Manufacturing
This is a B2B produced by Larry E Vaughn in 1988 for a medicine capsule manufacturer for use as a marketing tool.
Views: 212991 Larry E Vaughn
Manufacturing process of a medicinal product at Cinfa
All Cinfa's medicinal products are manufactured in high technology facilities under the most rigorous quality controls. In this video, you will see the whole process from the weighing and mixing of the active substances and excipients to the final tabletting and coating.
Views: 1500 Laboratorios Cinfa
Pharmaceutical tablet manufacturing process by wet granulation
This video explains pharmaceutical tablet manufacturing process by wet granulation process.
Views: 39044 Professor Tushar
Assembly Process Overview - Medical Device Manufacturing
B&A Health is a medical devices and pharmaceutical packaging contract manufacturing firm in Hyderabad, India. Our entire facility is equipped with cleanroom technology, ISO Class 8 in production area and ISO Class 7 in assembly, packaging and sterilization areas. This video showcases overview of assembly process followed at our facility. All the following processes are shown in the video: - Sub-Assembly - Assembly - Quality ----------------------------------------------------------------------------------------------------------- Music Credits - Song By Adam Vitovsky
Views: 6339 B&A Health
Ifotam Co. Ltd. - active pharmaceutical ingredients
Ifotam -- Clever synthesis for demanding pharmacy. Ifotam CO.Ltd is one of the first spin off type companies in Poland, created on the basis of knowledge and experience of the research staff of the Center of Molecular and Macromolecular Studies (Polish Academy of Sciences, Lodz) and the Pharmaceutical Institute (Warsaw). The company was founded in 1989. Our activities are focused on search for, and development of, new methods of synthesis, transfer of technologies, production of APIs and sales of pharmaceutical substances. Many years of work on the company development have resulted in our current position of the one of more important manufacturers of first generation cytostatics in Europe. We specialize in synthesis of three groups of pharmaceuticals: - drugs used in anticancer therapies, - drugs used in treatment of skeletal system disorders, - protective drugs -- used in antitumor chemotherapy. On request of our clients, we also perform custom syntheses. Two production sites located in Łódź, with their laboratory and production facilities, allow to manufacture active pharmaceutical ingredients in quantities ranging from a few grams to 2 tonnes. Ifotam has at its disposal own, modern research and development laboratories, which enable us to launch new products efficiently, effectively and in a short time. Our highly qualified R&D Department staff makes it possible to develop new ideas as well as to search for, and to implement innovative solutions. That dynamically developing department of our company can take pride in numerous achievements and patents in the field of chemical synthesis, which have contributed to high quality and efficiency of our products. Ifotam has been also cooperating for many years with scientific institutions and research centers all over the world, which enables quick implementation of the latest advances in production of APIs. The products manufactured by Ifotam meet the requirements of current GMP. Owing to precise implementation of, and strict compliance with the GMP requirements, we gained the approval of FDA as early as 2001. We were one of the first companies in Poland positively assessed by international auditors. The active substances are manufactured in production centers specially designed for this purpose. Each substance is manufactured in the dedicated premises and the dedicated apparatus is used. High quality of our products, maintained consistently over a period of 20 years, is our asset. Our Quality Control Laboratory is responsible for monitoring the quality of products sold by us. The substrates using in the manufacturing processes, intermediates and final products are controlled there. All the procedures and instructions are based on the GMP guidelines. The Laboratory has analytical equipment allowing to perform all analyses in compliance with the Polish, European and US Pharmacopoeias. Ifotam is associated, first of all, with innovation, quality and timely delivery of products. We are a dynamically developing Polish enterprise supplying pharmaceutical companies all over the world. It is confirmed by the fact that export accounts for as much as 80% of our sales. We care about the satisfaction of our clients on such demanding markets as the USA, Germany, or Russia. Our partners have been cooperating with us with satisfaction for over 10 years. We supply products meeting the strict standards of the pharmaceutical market. Our products are: ifosfamide, cyclophosphamide, zoledronic acid, pamidronate disodium, risedronate sodium and others.
Views: 14098 Ifotam Co. Ltd.
Inside the Indian Generic Drug Manufacturer Cipla
India produces over 30% of the world's entire supply of generic drugs. Cipla is one of India's largest drug manufacturers. It supplies antiretroviral drugs to about one third of AIDS patients under treatment in Africa. C&EN Senior Correspondent Jean-François Tremblay went inside Cipla's advanced pharmaceutical ingredient manufacturing plant to learn more about the stringent regulations it must follow. India's future as the world's drugstore is a controversial topic. Other drugmakers have been heavily fined, or had products recalled or banned, because of problems at plants. And India is under pressure to make its patent system more like those in western nations. But India has found a market for low-cost drugs and that market isn't about to disappear. More at http://cenm.ag/cpla Like C&EN? Want more chemistry video goodness? Subscribe to our YouTube channel: https://www.youtube.com/user/CENonline Subscribe to C&EN to watch science videos with a focus on chemistry, and to hear from the researchers behind it all. -- Looking for C&EN elsewhere on the internet? Homepage: http://cen.acs.org Facebook: http://www.facebook.com/CENews Twitter: http://www.twitter.com/cenmag Tumblr: http://cenwatchglass.tumblr.com
Views: 77947 CEN Online
Capsules Manufacturing process IN PHARMACEUTICALS
In the manufacture of pharmaceuticals, encapsulation refers to a range of dosage forms—techniques used to enclose medicines—in a relatively stable shell known as a capsule, allowing them to, for example, be taken orally or be used as suppositories. The two main types of capsules are: Hard-shelled capsules, which contain dry, powdered ingredients or miniature pellets made by e.g. processes of extrusion or spheronization. These are made in two halves: a smaller-diameter “body” that is filled and then sealed using a larger-diameter “cap”. Soft-shelled capsules, primarily used for oils and for active ingredients that are dissolved or suspended in oil. Both of these classes of capsules are made from aqueous solutions of gelling agents, such as animal protein (mainly gelatin) or plant polysaccharides or their derivatives (such as carrageenans and modified forms of starch and cellulose). Other ingredients can be added to the gelling agent solution including plasticizers such as glycerin or sorbitol to decrease the capsule's hardness, coloring agents, preservatives, disintegrants, lubricants and surface treatment. Since their inception, capsules have been viewed by consumers as the most efficient method of taking medication. For this reason, producers of drugs such as OTC analgesics wanting to emphasize the strength of their product developed the “caplet”, a portmanteau of “capsule-shaped tablet”[1], in order to tie this positive association to more efficiently-produced tablet pills, as well as being an easier-to-swallow shape than the usual disk-shaped tablet.
Views: 313 Pharmansh
Video: Teva Parenteral Pharmaceuticals
Client: Teva Parenteral Pharmaceuticals
 Title: "The Essential Piece"
 Objective: Convince each employee that he or she is an integral vital part of the whole at Teva. Background: Winner of a Telly Award for excellence in video creative and production.
Views: 13677 MedMenBeardboy
Pharmaceutical Product Manufacturing Companies In India
Rablon healthcare pvt ltd launching the new products soon with great range of medicine.It is the best supplier of branded medicines,which distributes its products all over the world. Visit us online at : http://www.rablon.com/
Views: 1589 James Thomas
Lifecycle Approach to API Process Validation
The goal of API process validation is to ensure the reliable production of high-quality active pharmaceutical ingredients from development through commercialization. The product lifecycle approach established in FDA's 2011 Process Validation Guidance requires different validation activities during the process design and process qualification stages, as well as continued process verification throughout the life of the commercial process. The process validation needs for pre-qualification activities and ongoing process verification can be daunting, especially for small and medium-size pharmaceutical companies. In this webinar, experts on API process validation outline the key requirements for development of a phase appropriate manufacturing plan including regulatory requirements, data collection, specification development, critical process parameters, sampling plans, and analytical method validation. Key Learning Objectives: * Understand the regulatory expectations at each clinical phase. * Determine the key validation aspects of API manufacturing including critical process parameters. * Identify analytical and stability needs as the API advances in the clinic. Moderator: Rita Peters Editorial Director Pharmaceutical Technology Speakers: Paul Wrezel, Ph.D. Director of Analytical Method Development Regis Technologies Bikash Chatterjee President and Chief Technology Officer Pharmatech Associates Inc. Paul L. Pluta, PhD Editor-in-Chief Journal of GXP Compliance and Journal of Validation Technology
Views: 12840 Regis Technologies Inc
Generic Drugs: Learn about the Lifecycle from Brand Name Prescriptions to Generics
Ever wonder why generic drugs cost $4 at some pharmacies? Generic drugs are the final stage in a long lifecycle that starts with innovator biopharmaceutical research companies researching and developing brand prescription medicines. This video highlights the stops & starts, successes & failures that often result in low-cost options for many people. Keep in mind as you watch that only 2 out of 10 drugs approved by the FDA will ever earn revenues that exceed average R&D costs. Help others understand the story behind the prescription drug lifecycle by sharing this video.
Views: 47152 PhRMAPress
How Sterile Solutions are Produced
Intravenous (IV) and other sterile pharmaceutical solutions are critical to virtually every aspect of treatment in a health care setting. As a leading manufacturer of IV and other pharmaceutical solutions in the U.S., Baxter has been a continuous supplier of these vital products for more than 80 years. Making IVs and other sterile solutions is complex and time-intensive, requiring the highest standards in quality and safety.
Views: 18737 BaxterInternational
Drug discovery and development process
Discovering and bringing one new drug to the market typically takes an average of 14 years of research and clinical development efforts. Learn about the many different steps in the complex drug discovery and development process. © 2011 Novartis AG
Views: 205719 Novartis
Taj Pharmaceuticals Limited (Full Manufacturing Process) {taj pharmaceuticals limited: mumbai}
taj pharmaceutical industry, taj pharmaceutical company, taj pharmaceutical companies, taj pharmaceutical manufacturer, taj pharmaceutical products, taj pharmaceutical exporter, manufacturers of taj pharmaceuticals, Taj pharmaceuticals chemicals Api Agro Products, taj pharmaceutical manufacturer india, manufacturer of taj pharmaceuticals, taj pharmaceutical injection, taj pharmaceutical injections, taj pharmaceuticals generics manufacturer india Taj Pharma (Full Manufacturing Process) Part-1 Our products hold the cure ( Get Healthy living From Taj Pharma) 1. What is a generic drug? A generic drug is loosely defined as a “copy” of a brand name drug. The active ingredient or drug content is identical or “bioequivalent,” and works in the body the same way as the brand name drug. Such drugs must show that their active ingredients get to the bloodstream at the same time and to the same extent as the brand name version. Generics are similar to brand name drugs in several other ways. These include the quality of the product, how it’s absorbed in the body, the dosage form (meaning if it is a pill, inhaler, or liquid), safety, dose strength, the way it is administered (or in other words, whether it’s taken orally, injection, etc.), the way it performs (whether immediate or controlled release), and also the FDA-approved use. The U.S. Food and Drug Administration, or FDA, approves generics based on not only some, but ALL of these standards. 2. Are generic drugs as safe and effective as brand drugs? Yes. Drug companies must prove to the FDA that the generic drug is either identical or otherwise bioequivalent to the brand drug, meaning they have the same quality, strength, purity and stability. The FDA allows for small variations in flavor, color, packaging, and a few other parameters to account for variability during manufacturing. FDA limits how much variability is acceptable Get Healthy Stay Healthy for more information on Your Health www.tajpharma.com / www.tajgenerics.com Copyright © 2004-2018 Taj Pharma (LIFE TIME SHO) TV. All rights reserved. This information—including product information—is intended only for YouTube Viewers. © LIFETIMESHO HD
Views: 63 Taj Pharma Life
Making Medicine - How Tablets are Made - Naked Engineering
We visit the tablet manufactuing site of Glaxosmithkline to see how millions of tablets are made each year with accurate precision for the global drug market...
Views: 163075 NakedScientists
Manufacturing of Pharmaceutical Bulk Drugs and Medicine
Manufacturing of Pharmaceutical Bulk Drugs and Medicine. Investment Opportunities in the Pharmaceutical Sector India is already among the top six producers of pharmaceuticals of the world. The Government of India has made tax breaks available to the pharmaceutical sector and a weighted tax deduction of 150 per cent for any R&D expenditure incurred. This is in league with Indian Government's Pharma Vision 2020 which aims at making India a global leader in end-to-end manufacture by 2020. India is home to 10,500 manufacturing units and over 3,000 pharma companies. India exports all forms of pharmaceuticals from APIs to formulations, both in modern medicine and traditional Indian medicines. Globally India ranks among the top exporters of formulations by volumes. For the majority of firms in this industry, the actual manufacture of drugs is the last stage in a lengthy process that begins with scientific research to discover new products and to improve or modify existing ones. The R&D departments in pharmaceutical and medicine manufacturing firms start this process by seeking and rapidly testing libraries of thousands to millions of new chemical compounds with the potential to prevent, combat, or alleviate symptoms of diseases or other health problems. See more http://goo.gl/1sQLwS http://goo.gl/jajeNa http://goo.gl/0tvlst Contact us: Niir Project Consultancy Services 106-E, Kamla Nagar, Near Spark Mall, New Delhi-110007, India. Email: [email protected] , [email protected] Tel: +91-11-23843955, 23845654, 23845886, 8800733955 Mobile: +91-9811043595 Fax: +91-11-23841561 Website : http://www.niir.org http://www.entrepreneurindia.co Tags Pharmaceutical Technology Books, Essentials of Pharmaceutical Technology, Pharmaceutical Technology, Pharmaceutical books, Science, Technology & Medicine Books, Drugs technology books, Drug and Pharmaceuticals technology book, Best small and cottage scale industries, Bulk Drugs Formulation, Bulk Drugs Manufacturing Industry, Business consultancy, Business consultant, Business guidance for Pharmaceutical industry, Business guidance to clients, Business Plan for a Startup Business, Business start-up, Creating a Pharma Start-up, Drug formulation manual, Formulation of Antibiotics, Formulation of Paracetamol, Formulation of Tablets, Great Opportunity for Startup, How to Start a Medicines manufacturing business?, How to start a pharmaceutical company, How to Start a Pharmaceutical Product Business, How to Start a Pharmaceutical Production Business, How to start a pharmacy business, How to start a successful drugs making business, How to start Antibiotics manufacturing business, How to start drugs pharmaceutical business, How to start medicine business, How to Start Medicine Manufacturing Industry in India, How to start medicine manufacturing, How to start Paracetamol production business, How to Start Pharmaceutical Manufacturing Company in India, Invest to setup a pharmaceutical business, Manufacturing of medicinal products- Pharmaceutical industry, Medicine Manufacturing Industry, Medicines Making Small Business Manufacturing, Modern small and cottage scale industries, Most Profitable Bulk Drugs production Business Ideas, New small scale ideas in Pharmaceutical industry, Pharma Manufacturing, Pharmaceutical and Medicines production Business, Pharmaceutical Based Profitable Projects, Pharmaceutical Based Small Scale Industries Projects, Pharmaceutical Drug Formulation, Pharmaceutical Drug Manufacturing Business, Pharmaceutical formulation guidelines, Pharmaceutical formulation, Pharmaceutical industry in India, Pharmaceutical industry, Pharmaceutical manufacturing Industry in India, Pharmaceutical Manufacturing Industry, Pharmaceutical Projects, Pharmaceutical, Bulk Drugs and Medicine Manufacturing Industry, Preparation of Project Profiles, Process technology books, Production in pharmaceutical industry, Production of Antibiotics, Production of cholera vaccine in fermentor, Production of Paracetamol, Production of Tablet, Profitable small and cottage scale industries, Profitable Small Scale tablets and drugs manufacturing, Project for startups, Project identification and selection, Quality Control: Tablet, Paracetamol, Antibiotics, Setting up and opening your Tablets production Business, Small Scale Bulk Drugs Manufacturing Projects, Small scale Commercial medicines making, Small scale pharmaceutical manufacturing, Small scale Pharmaceutical production line, Small Start-up Business Project, Start Bulk Drugs production business, Start Up India, Stand Up India, Starting a Pharmaceutical Manufacturing Business, Start-up Business Plan for Pharmaceutical industry, Startup ideas, Startup Project for Pharmaceutical industry, Startup project plan, Startup Project, Startup, Tablets making machine factory
Part 3 USANA's manufacturing process apart—from pharmaceutical-level GMPs to process validation
Manufacturing Excellence: Setting the Standard, Setting Us Apart By David Baker Talk of manufacturing facilities bring a few images to mind. You have the greasy, grinding gears of industry sending out sparks and soot, or Willy Wonka's chocolate river flowing through a pastoral candy paradise. Fortunately, USANA's in-house manufacturing facilities are neither industrial wasteland nor cartoonish wonderland. Walking the path of a USANA product brings you through clean, sterile environments, past operators dressed in full regalia, and through impressive, shiny machinery. Every step of the journey—from the powders dumped into a room-sized cone mixer to the multi-layer tablet press machine-gunning out finished products—is designed to maximize quality. (See the video below to follow a product on its path from powder to pill.) For years, USANA voluntarily adhered to pharmaceutical-level Good Manufacturing Practices (GMPs). Recently, USANA took another step and acquired U.S. Food and Drug Administration (FDA) Drug Establishment Registration. Now, USANA's facility can be inspected under pharmaceutical guidelines—the FDA's highest possible standard for manufacturers. No changes need to be made to USANA processes in order to comply with the increased FDA scrutiny. Along with adhering to pharmaceutical-level GMPs, the manufacturing process for each product is fully validated. "Our validation process ensures that we know how to manufacture a batch of tablets with tablet-to-tablet ingredient uniformity," said Dr. John Cuomo, USANA's executive director of research and development. "We know, for example, if we're making Mega Antioxidant we not only match the labeled amount of ingredients in a bottle, but that each and every tablet in that batch has those ingredients at the labeled amount, with very little variation. I don't think anybody else in the nutraceutical industry is doing that. Certainly not anybody who doesn't do the production themselves." Validation means establishing checks throughout the system and testing at different points in the process. This also means mixing up anywhere from 600 to 1500 kilograms of different powders and putting them in a big blender and making tablets so you can test a representative sample of a full production run. Basically, process validation is a very big, very expensive experiment, Dr. Cuomo says. But it assures you are making a consistent product that contains the right ingredients, in the right quantities, uniformly through a batch. The validation process is only done once or twice on a product to set up the parameters and procedures for making that product properly. However, every commercial batch of products made in USANA's manufacturing facility go through weight uniformity testing, as well as a variety of tests on the final product. Since the process has been validated and there are checks established throughout the system, any problems can be recognized and dealt with immediately. Knowing the proper processes and having control over every step from raw material to tablet gives USANA unmatched quality control, which shows in each and every product. Having control over every step gives USANA unmatched quality control, which shows in each and every product. "I haven't come across any of our direct competitors who have the same kind of facility and can manufacture their own products like we do," said Dr. Mark Brown, USANA's director of product development. "We took a good process and made continuous improvements to it over the next 20 years. We have a very solid operation and I think that's the number-one key to assuring a quality product." This production of quality products has been a cornerstone of USANA since its founding in 1992. "Quality manufacturing is important because we're trying to provide products that actually do something for people," Dr. Cuomo said. "We really believe in Dr. Wentz' vision that you can provide people with the proper nutrients to help maintain optimal health. To do that, you've got to give them products that are proven and tested, and you've got to make sure that you're getting the right material into the finished product, and nothing else." Tell us what you think about this Manufacturing Excellence series at [email protected] Watch this video about USANA's manufacturing process.
Views: 4811 diabetes1008
Inner Box for Pharmaceutical Product   manufacturing date, expiry date and lot number
www.ptasia.asia | Inner Box for Pharmaceutical Product manufacturing date, expiry date and lot number The Sriprasit story began in 1949. At that time, five siblings decided to set up their own family business in the Watsampluem district of Bangkok, having gained experience from working in other pharmacies. Sriprasit Dispensary R.O.P. was established, started out as a small pharmacy. A few years later it was one of the first companies to import pharmaceutical products from abroad. To expand the range of products and pave the way for market expansion, in 1975, Sriprasit Pharma Co., Ltd. was set up to manufacture pharmaceutical products. The company continues to manufacture such products under supervision of the experts. Its products were distributed by Sriprasit Dispensary. Sriprasit Dispensary and Sriprasit Pharma have since become one of the leading importers, manufacturers, distributors and exporters of pharmaceutical products. Sriprasit Pharma's products are exported to South East Asian countries such as Malaysia, Singapore, Laos and Myanmar and South Africa. Sriprasit Pharma was among the first group in Thailand that adopted the GMP standard of pharmaceutical manufacture in 1989, and later was awarded the ISO 9001 version 2000 standard. The company has a policy of maintaining and developing quality standards that are recognized internationally. Sriprasit Pharma's products come in tablets, capsules, liquids, creams and ointments. All production processes meet strict quality control standards. Hygienic inspection is regularly imposed in every manufacturing facility. Pharmaceutical raw materials used come from the best chemical sources such as those in Switzerland, Germany, France, Italy, USA, Japan, etc. New products are constantly being researched and developed in response to the growing demand from the pharmaceutical markets, both at home and abroad. Strictly following international manufacturing standards of the GMP and ISO, Sriprasit Group is trusted in all aspects of the medical and pharmaceutical fields, including state and private hospitals and medical schools.
Views: 1375 HSAJET TIJ
Theon Pharmaceuticals Ltd
Theon Pharmaceuticals Limited: Building Hopes spreading Happiness!! Theon is located in lush-green, serene and excise free zone of Nalagarh in the state of Himachal Pradesh, India. Theon is ISO 9001:2008, WHO-GMP certified company. The company has its strong presence in high growth therapeutic segments of Cardiology, Diabetology, Anti depressant, Anti-allergic, Anti- infective, antacid, Anti-virals, Anti-bacterials, Decongestants, Anti-epileptics, Muscle Relaxants Theon is equipped for manufacturing solid oral & dry syrup formulations with installed plant capacity of about 1000 Million & 700 Million units respectively per annum. Right from the state-of-the-art manufacturing expertise, Theon has dedicated and segregated blocks for General, Pencillins & Cephalosporin (Beta Lactums), Carbapenems, oral dosages in the form of tablets, Capsules and Dry Syrups covering major therapeutic segments. To harness global opportunities and ongoing expansion spree, Theon has carved its niche in Dry Powder Injectables with its new ultra-modern facility designed with exacting standards of MHRA, TGA, MCC, ANVISA. The facility is caters to International and Domestic Markets with a massive capacity of 100 million DPI/annum. Theon is sensitive to the quality needs and strictly adheres c-GMP norms, possess with Automated equipment operated with pre-programmed logic controllers like:  Automatic Vial Washing Machine  Sterilizing & dehydrogenating Systems  Filling & stoppering Machines  Labeling with auto cartoner Theon has multicultural, multilingual and motivated professionals of more than 800 employees, we, at Theon strongly believe in "Customer Centricity" and count our milestones with the number of satisfied customers we have. We believe in building a long-term relationship with our patrons by delivering them services, which exceeds their satisfaction level. Our esteemed clients list includes: Cadila, Ranbaxy, Cipla, Wockhardt, Mankind, Elder, Ajanta, Abbott, Medley, Meyer, Macleod's and many more all over India. Quality and innovation are the hallmark of Theon. Equipped with latest sophisticated instruments in its in-house chemical, instrument and microbiological laboratories Complying with schedule L, Supported by a large pool, of scientists who continuously work towards new pharma products. Our every product is checked thoroughly and passed through stringent quality tests, as we achieve constant compliance to produce quality attributes with cost efficiency Theon's manufacturing facility is equipped with Automatic access control system at process area to ensure entry of only authorized personnel. At Theon we strongly support Environmentalism, and keeping in mind the same. We use innovative Method & Technology to have highest standards of Safety, Environment and Health in our manufacturing processes. All the utilities equipped at Theon have been procured from reputed suppliers. Theon has marked its presence globally by exporting its products to practically every continent which includes Africa, CIS countries, Latin America, & Asia pacific. We have dedicated Export regulatory department team, which ensures and facilitates international audits, documentation, COPP, dossier preparations as per ACTD and CTD format in total compliance with c-GMP norms. At Theon Pharma it is our endeavour to continuously develop new products, processes, technology and look out for new horizons in pharmaceutical business. We are committed to move ahead and give our unflinching efforts, support and dedication for the service of humanity by developing innovative, therapies hence making healthier and happier world.
Views: 23516 Harwinder Singh
Dispensing API materials safely using a downflow booth and a dispensing isolator
Contact us for more information on your pharmaceutical manufacturing processes and how we can make then safe for your operators and your products. We're happy to advise on any aseptic or containment issues you might have. Contact us at [email protected] or ring through to relevant numbers that you can find here: http://extract-technology.com/contact/contact-us/
Views: 8121 Extract Technology
The FDA Drug Development Process: GLP, GMP and GCP Regulations
This Video provides an overview of the FDA's Drug Development Process. This webinar also includes the major FDA regulations involved in the Drug Development Process - the GLP, GMP and GCP regulations. This Video is ideal for those who are new to the Drug Development process and those experienced researchers that need an update on FDA requirements. This webinar will address the basic Drug Development Process, nonclinical trials and human clinical trials. In addition the two major FDA submissions during Drug Development will be covered - the IND submission and the NDA submission. For More Information Contact - Organization: NetZealous BDA GlobalCompliancePanel Website: http://www.globalcompliancepanel.com/ Email: [email protected] Help us caption & translate this video! http://amara.org/v/JGhy/
Views: 23965 GlobalCompliance Panel
Clinical & Product Development Process - Custom Pharma Services Ltd
An animated guide to the Clinical & Product Development capabilities of Custom Pharma Services, UK. We are a contract development and manufacturing organisation (CDMO). We serves other companies in the pharmaceutical industry on a contract basis to provide comprehensive services from drug development through to commercial manufacturing. From manufacturing small batches for clinical trials to scaling up for mass production and worldwide distribution, Custom Can! Find out more at: http://www.custompharma.co.uk/services/clinical-development/
Views: 229 Custom Pharma
Contract Pharma Manufacturing & Packaging
Is your organization looking for pharmaceutical contract manufacturing and packaging? At WellSpring, we may be able to help...
Glenmark Pharma Entry & Exit Video
this video shows primary & secondary gowning and entry & exit procedure training for employees at Glenmark Pharmaceutical Limited
Views: 146306 cyber monk
VITRONIC - VINSPEC HEALTHCARE - Track and Trace - Quality Inspection of Pharmaceutical Products
VINSPEChealthcare Track and Trace enables secure labeling, identification, tracking, and quality inspection of pharmaceutical products. A tightening of the regulations to combat counterfeit medicinal products in many countries means that maximum security in the supply chain is essential in the manufacturing of pharmaceutical products. Serialization to ensure the unique traceability of products is becoming a critical quality and security requirement. That's why traceable data must be assigned to products during every phase of the production and packaging process. VITRONIC's Track & Trace solution from the VINSPEChealthcare range ensures reliable serialization of pharmaceutical products. Traceability is guaranteed thanks to the logical linking of all product and packaging units. In accordance with the EU Falsified Medicines Directive 2011/62/EU, all EU Member States are required to establish a system to safeguard against the counterfeiting of pharmaceutical products by 2017. Similar restrictions apply to the pharmaceutical industry across the globe, e.g. in the USA, China and Brazil. Pharmaceutical manufacturers in those countries are always required to assign unique, traceable serial numbers to all of their products and packaging units. The new system will make all pharmaceutical products be fully traceable all the way from the manufacturer to the customer. VINSPEChealthcare Track & Trace encodes serial numbers, checks that they are put onto products correctly, and aggregates across various packaging units. Automatic serialization With the Track & Trace solution, essential information such as product number, batch ID and expiry date are simultaneously placed on the product in both plain text and barcode form. Once the information has been assigned to and put onto the products, the Track & Trace system checks that the information is both correct and complete. This essential information is stored, so that products with defective barcodes can be detected and rejected. Seamless traceability thanks to aggregation With VINSPEChealthcare Track & Trace inspection solutions, serial numbers can be encoded, put on products, inspected and captured for each individual product and at all subsequent levels of packaging, from multi-packs to shipping pallets. The data from all packaging units is transferred to a central line database, where data records are linked together logically. Based on this aggregation, the manufacturer can then accurately track the entire production history of an item. All of the data that is collected and aggregated is transferred to the existing MES and ERP systems. As a result, statutory requirements can be fulfilled, and analyses, reports and process optimizations implemented quickly and in real time. Quality inspection In addition to ensuring accurate aggregation and seamless traceability of pharmaceutical products, VINSPEChealthcare Track & Trace systems allow GAMP-compliant quality inspections to be conducted at the same time as Track&Trace during the production and packaging process. Optical contour, surface and dimensional inspections, plus the detection of defective packaging, can be implemented inline and at high throughput. GAMP qualification package We also offer an optional GAMP qualification package for VINSPEChealthcare Track & Trace systems. For assistance please visit our website: https://www.vitronic.com/industrial-and-logistics-automation/sectors/medicine-pharmacy/track-and-trace.html
Developing and Delivering Pharmaceutical Products: Four Hot Tips for Start-ups
Colin Minchom, President, Cordack Inc., shares tips for successfully steering through the pharmaceutical product development (CMC) process.
Made In India-Pharmaceutical Industry-2015
The Pharmaceutical industry in India is the world's third-largest in terms of volume. According to Department of Pharmaceuticals the total turnover of India's pharmaceuticals industry between 2008 and 2009 was US$21.04 billion. India is one of the fastest-growing pharmaceutical markets in the world and has established itself as a global manufacturing and research hub. A large raw material base and the availability of a skilled workforce gives the industry a definite competitive advantage. India is today one of the top emerging markets in the global pharmaceutical scene. The sector is highly knowledge based and its steady growth is positively affecting the Indian economy. The organized nature of the Indian pharmaceutical industry is attracting several companies that are finding it viable to increase their operations in the country. In 2013, there were 4,655 pharmaceutical manufacturing plants in all of India, employing over 345 thousand people The government of India started to encourage the growth of drug manufacturing by Indian companies in the early 1960s, and with the Patents Act in 1970. However, economic liberalization in 1990s enabled the industry to flourish. Indian companies carved a niiche in both the Indian and world markets with their expertise in engineering new processes for manufacturing drugs at low costs. Although some of the larger companies have taken small steps towards drug research and innovation, the industry as a whole has been following this business model until the present. The Indian pharmaceutical industry was estimated to be worth US$ 23 billion in 2 thousand 10 and is expected to touch US$ 55 billion by 2016. Globally, India ranks third in terms of volume of production and fourteenth largest by value. The domestic market is likely to grow from US$ 13 billion in 2010 to US$ 25 billion by 2017. The domestic pharma sector is witnessing strong growth due to higher penetration in tier-2 and tier-3 cities and greater focus on the largely- untapped rural market. The major factors responsible for this growth are increasing sales of generic medicines, continued growth in chronic therapies and greater penetration in rural markets. India exports to more than 200 countries; its share of exports is expected to grow incrementally. Pharmaceutical exports grew from US$ 8.6 billion in 2008 to US$ 14.5 billion in 2012, at a rate of 13.8 per cent. The US is India’s largest importer. The exports to the US grew at a rate of around 24 per cent between 2006 and 2010. The export of bulk drugs continue to grow to regulated markets and is supported by India’s existing foothold in semi-regulated market. India currently exports drug intermediates, Active Pharmaceutical Ingredients, Finished Dosage Formulations Bio-Pharmaceuticals, and Clinical Services across the globe. The exports of pharmaceuticals from India grew to US$ 14.6 billion in 2012from US$ 6.23 billion in 2006, registering a compound annual growth rate of around 15.2 per cent. India, with almost 200, US FDA drug manufacturing facilities, is the biggest foreign supplier of medicines to the United States . Exports to the US rose nearly 32 per cent last year to US$ 4.23 billion. India accounts for nearly 40 per cent of generic drugs and over-the-counter products and 10 per cent of finished dosages used in the US. Generic drugs have a dominant position in the rapidly expanding Indian drug industry. India's exports of generic drugs have been growing at a rate of 24 per cent over the past four years. In the period 2002 to 2012, the country’s healthcare sector grew 3 times in size, touching US$ 70 billion from US$ 23 billion. The Top 10 Publicly Listed pharma companies in India by Market Capitalization as of 2015 are Sun Pharmaceutical, Lupin Pharmaceuticals, Dr. Reddy's Labs, Cipla, Aurobindo Pharmaceutical, Cadila Healthcare, Glenmark Pharmaceuticals, Divis Labs and Torrent Pharmaceuticals. The Indian pharma industry is on a good growth path and is likely to be in the top 10 global markets in value terms by 2 thousand 20, according to the Price water cooper report. High burden of disease, good economic growth leading to higher disposable incomes, improvements in healthcare infrastructure and improved healthcare financing are driving growth in the domestic market, the report highlighted. The small and medium enterprises are expected to play a significant role in the growth story of the country's pharma sector as they contribute 35–40 per cent to the industry in terms of production
Views: 34803 KoSh Films
Purdue's Continuous Tableting Line
https://engineering.purdue.edu/CP3 For students pursuing careers in the pharmaceutical industry, it can be difficult to put theories and computer models into practice. At Purdue, they can actually operate a Continuous Tableting Line: a full downstream production plant creating up to 1600 pills a minute. Students can experiment and measure different powder mixtures, granulations, flow rates, and manufacturing processes. They can also test the resulting tablets for hardness, consistency, size, and effectiveness in different environments. Read more about the Designer Particulate Products preeminent team: http://bit.ly/discovery-particles Mariana Moreno and Sudarshan Ganesh are Chemical Engineering graduate students, studying under G.V. (Rex) Reklaitis and Zoltan Nagy. Yasasvi Bommireddy is a Mechanical Engineering graduate student, studying under Marcial Gonzalez. Chemical Engineering: http://engineering.purdue.edu/ChE Mechanical Engineering: http://engineering.purdue.edu/ME The pilot plant is part of the Center for Structured Organic Particulate Systems (C-SOPS), funded by the National Science Foundation. Center for Particulate Products and Processes: https://engineering.purdue.edu/CP3
How to know about Good Manufacturing Practices in Telugu || GMP Guidelines In Pharma || Pharma Guide
How to know about Good Manufacturing Practices in Telugu || GMP Guidelines In Pharma || Pharma Guide • Here we are discussing about good manufacturing practices. • A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. • GMP designed to minimise the risks involved in any pharmaceutical production, that cannot be eliminated through testing the final product. • Some of the rules and regulations of GMP are, • Writing step by step Standard Operating Procedures and work instructions. • Then following written procedures and instructions. • Documenting our work. • Validating our work. • Designing and constructing facilities and equipment. • Protecting against contamination. • Controlling components and product related processes. • Conducting planned and periodic audits. #pharmaguideradhakrishna #PharmaGuide
Views: 21971 Pharma Guide

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