2 Day Seminar: Health Canada/USP/EP Raw Material Requirements in a cGMP Environment Issues and Solutions (Philadelphia, PA, United States - March 16-17, 2023)
10 Feb 2023
Executive Change
DUBLIN, Feb. 10, 2023 /PRNewswire/ -- The "Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions" training has been added to
ResearchAndMarkets.com's offering.
Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms and gene therapy products, as few as fifteen to twenty or as many as sixty raw materials need to be sourced before the process can be moved from initiation through completion.
The objective of this seminar is to explore raw materials and their requirements - issues and solutions. It will also explore how water impacts the final product since water is the single largest raw material that is used within most processes.
Another objective is to assure that your organization is maintaining itself within a cGMP compliance framework to include ICH Q7, Q9 and Q11. Case studies to include Warning Letters will be discussed to illustrate regulatory raw material issues.
This highly interactive two day seminar on raw material requirements in a cGMP environment will:
Compare and Contrast FDA, Health Canada, ICH, USP and EP requirements
Review latest updates to include FDA, Health Canada, ICH, USP and EP requirements
Examine a variety of the issues surrounding raw materials to include what materials should be tested and to what extent during Phase 1, 2, 3 and commercial production.
Cover testing requirements during each Phase (Phase appropriate), to include microbial and endotoxin, and what may be optional (regulatory risk) until the product moves to its next Phase.
Determine what options exist - even within a Phase 2 or Phase 3 testing framework.
Discuss compendial vs. non-compendial testing and how to respond when no method is available.
Discuss how a 90 percent vs. a 90.0 percent minimum purity analysis can delay initiation of testing.
Explore the number of lots required for testing before reduced testing might occur and why some companies don't accept this route.
Review the use of individual samples vs. composite samples for testing.
Review packaging and storage requirements and their impact on in-coming materials to include both raw materials and API.
Explore ASQ testing to include how to choose attributes and sample size.
Determine when the ASQ vs. square root of N+1 is appropriate.
Learning Objectives:
Upon completing this course on raw material requirements in a cGMP environment participants will:
Understand how various types of raw materials may impact the user.
Learn of the impact of raw materials to include any bacterial and endotoxin issues in the timely production of a product.
Determine the single most used raw material in large molecule production and what it means to the user.
Find the sources of analyses assistance for raw materials.
Appreciate the requirements for Phase 1 through commercial manufacturing - why safety is required as part of Phase 1
Initiation of additional testing -- when?
Examination of regulatory risk to include ICH Q7, Q9 and Q11.
Why use compendial testing in lieu non-compendial testing.
Testing requirements -- when is enough?
Understand packaging and storage requirements and their impact on in-coming materials to include both raw materials and API.
The impact of ASQ vs. square root of N+1 on sample size and attribute testing.
Who Should Attend:
Quality professionals
Regulatory professionals
Compliance professionals
Manufacturing engineers
Quality engineers
Quality auditors
Quality Control
Microbiology
In-coming Materials
Document control specialists
R & D
Project Managers
Agenda
DAY 01 (10:00 AM - 4:00 PM EST)
Compare and Contrast FDA, Health Canada, ICH, USP and EP requirements.
The various raw materials and the user impact
Impact of raw materials in the timely production of a product
The impact of the single most used raw material in large molecule production and its impact upon the user
The regulatory requirements for Phase 1 through commercial manufacturing
The use of additional testing - does one only review the C of A
DAY 02 (10:00 AM - 4:00 PM EST)
The use of compendial testing in lieu of non-compendial testing - pros and cons
Regulatory risk (ICH Q9) with raw materials
Testing requirements - how to sample
Testing requirements - how to test
The impact of ASQ and square root of N+1 on sample size and attribute testing
Case Studies - Time to apply the previous two days
Warning Letter examples
Speakers:
Barry A. Friedman, Ph.D
Consultant
Dr. Friedman possesses over 30 years of industrial managerial experience in various aspects of biopharmaceuticals and medical devices to include regulatory compliance, expert witness testimony, GLP/GMP, quality control, auditing, sterility assurance, microbiological/analytical validations and fermentation technology.
Prior to becoming an independent consultant, Dr. Friedman was associated with Cambrex Bio Sciences, a contract manufacturer of GMP bulk biopharmaceuticals located in Baltimore, Maryland. As the Director of Quality Control, he managed a multi-shift Department of thirty one individuals involved in client management, the receipt and testing of raw materials, environmental monitoring and microbiology, analytical chemistry and QC compliance for the production of Phase 1, 2, 3 and commercial products manufactured from bacteria, yeast and mammalian cells. In this capacity, Dr Friedman enjoyed many client and regulatory interactions, both domestic and international.
Prior to 2000, Dr. Friedman was the Laboratory Director for Chesapeake Biological Laboratories, a contract Aseptic Fill n' Finish manufacturer located in Baltimore, Maryland. In addition to the professional history listed above, other associations have included W.R. Grace, Sigma Chemical Co., Sherwood Medical, Becton Dickinson, American Cyanamid and Union Carbide.
Dr. Friedman received his B.S. degree in Microbiology from Ohio State University, his M.S. from Michigan State University in Microbial Genetics, and his PhD from Ohio State University in Microbiology.
For more information about this training visit https://www.researchandmarkets.com/r/rf1ttx-material?w=5
About ResearchAndMarkets.com
ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.
Media Contact:
Research and Markets
Laura Wood, Senior Manager
[email protected]
For E.S.T Office Hours Call +1-917-300-0470
For U.S./CAN Toll Free Call +1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Logo: https://mma.prnewswire.com/media/539438/Research_and_Markets_Logo.jpg
SOURCE Research and Markets
For more details,please visit the original website
The content of the article does not represent any opinions of Synapse and its affiliated companies. If there is any copyright infringement or error, please contact us, and we will deal with it within 24 hours.
Indications
Targets
-Drugs
-Chat with Hiro
Hot reports
Get started for free today!
Accelerate Strategic R&D decision making with Synapse, PatSnap’s AI-powered Connected Innovation Intelligence Platform Built for Life Sciences Professionals.
Start your data trial now!
Synapse data is also accessible to external entities via APIs or data packages. Empower better decisions with the latest in pharmaceutical intelligence.