6-Hour Virtual Seminar
6-Hour Virtual Seminar on Phase I GMPs
08:00 AM PDT | 11:00 AM EDT
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Live: One Dial-in One Attendee
Corporate Live: Any number of participants
Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy subjects and use lower doses of the drug product.
Therefore, only small amounts of investigational material are required. In order to not undertake substantial costs and to reduce regulatory burden during these early stages, the FDA has established guidelines to allow early stage investigational products to be manufactured under less stringent GMPs.
This workshop will review the current regulations, guidance documents for early stage manufacturing and GMPs in detail. Regulatory strategies and logistical considerations for early development stage product, including vendor selection and management, stability, labeling, and documentation requirements will also be reviewed and explored.
Why you should Attend:
Attend this conference so that you may understand differences between GMP requirements for early and later stage clinical development. Explore and discuss ways to develop and implement strategies for early GMPs for phase I clinical studies.
Lecture 1 - The following topics will be discussed to provide the foundation and basis for advancing drugs into clinical development from research and providing required information to the FDA regarding these products.
- Moving a Product out of R&D
- CMC Requirements for an IND Study and commercial
- Good Manufacuring Practices: Basics for Beginners
- Raw Material Management
Specific topics include:
- Issues with research greade material used for laboratory and nonclinical testing
- Optimizing manufacturing processes
- Raw material requirements and process development
- Assessing scalability of manufacturing
- Planning the CMC for a potential IND
- Study Essential elements of the CMC section of an IND
- Characterization of the active ingredient and finished product
- Various kinds of products: drugs, biologics, botanicals, diagnostics, medical device
- Manufacturing facility personnel eqquipment and requirements
- Core principles of GMP regulatory requirements for all different products durgs to medical devices
- Customizing regulatory compliance to a given product
- Role of discussions with the FDA
- Planning for the early stage with an eye toward large scale manufacturing
- Vendor management
- Raw material handling issues for early stage products
- Manufacturing step development
Lecture 2 - The following topics will be discussed to provide the requirements for early stage products of different types and for vendor selection and management.
Who Will Benefit:
- The scope of the FDA guidance
- Acceptable practices and tips
- GMP requirements for exploratory clinical studies
- Specific requirements for drugs, biologic, and combination products
- Specific issues for various kinds of combination products
- Combination products with one or more new components
- CMC issues for 505(b)(2) products
- GMP and QSR: which to follow for a combination product
- Introduction to process validation for early stage manufacturers
- Step by step introductions for process validation
- Process validation reports and other documentation
- Developing SOPs based on valiidation processes
- Logistics of using contract manufacturing organizations for early stage products
- Pilot scale manufacturing requirements GMPgrade and nonGMP grade manufacturing
- Benefits and challenges with using local and international vendors
- Supervisors in Regulatory Affairs
- Quality Assurance
- Clinical Operations
Peggy J. Berry ,MBA, RAC, is the President & CEO at Synergy Consulting where she provides consulting services to companies in all aspects of drug development. She also provides group and one-on-one training in drug development, regulatory affairs and project management topics.
Prior to founding Synergy Consulting in 2015, she was Vice President of Regulatory Affairs at Insmed (2/2015-5/2015) where she was responsible for the development and implementation of global regulatory strategies and the management and oversight of the regulatory affairs department. Prior to Insmed, she was Vice President of Regulatory Affairs and Quality at Amarin (3/2009-2/2014).
She has also held a variety of senior level positions at Dyax (5/2006-3/2009), MGI Pharma (now Eisai; 7/2005-5/2006), AstraZeneca (10/2001-7/2005), and Dey Pharma (now Mylan; 12/1997-10/2001). She has also held Regulatory Affairs roles within two clinical contract research organizations (ILEX Oncology and Cato Research Ltd; 1992-1997) and has worked in review divisions at the FDA (1985-1992).
In addition, Ms. Berry consults for a number of companies in the regulatory and quality area, conducts a number of training courses, and is active in the Regulatory Affairs Professionals Society. She is the editor of the 2010 book "Choosing the Right Regulatory Career" (RAPS, MD) and author of the 2011 book "Communication & Negotiation" (RAPS, MD).