Good Laboratory Practice Regulations - Introduction and Strategies for Implementation - Recorded Webinar

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Webinar Duration: 60 minutes

RECORDED: Access recorded version only for one participant; unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of payment)

SPEAKER: Ludwig Huber

OVERVIEW:
Complying with GLP regulations can increase the cost of a laboratory up to 30%. Companies or employees either don't know exactly what GLP really means, what procedures are required and how to implement GLP regulations. Lack of GLP knowledge is also an inspection issue as training plans should include basic GLP knowledge for everybody working in a GLP environment This seminar will give a good understanding of GLP regulations and recommendations and tools for implementation.

Areas Covered in the Session:
- FDA and International GLP regulations: 21 CFR Part 58, OECD
- Objectives and concepts of GLP's
- Special organizational requirements
- Responsibilities: Management, Study director, QA, analysts
- SOP requirements: type, formats and enforcement
- GLP studies: preparation, conduct, documentation
- Key requirements for equipment, facilities reference material, people
- Data generation and evaluation: raw data, intermediate results, final results
- Records keeping: format, length of time, archiving and reprocessing

For easy implementation, Attendees will receive:
- Good Laboratory Practices and Current Good Manufacturing Practices: 120 pages e-book
- Gap Analysis/Checklist: Good Laboratory Practice Regulations
- SOP: Archiving GLP Data and Other Documents

Who Will Benefit:
- Supervisors and Managers
- QA managers and personnel
- GLP auditors
- GLP study directors
- Analysts
- Consultants
- Teachers

SPEAKER PROFILE:
Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems, Informa Healthcare". He has given more than 300 presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. For more information, please visit Dr. Huber’s website www.ludwig-huber.com

After your payment, we will contact you with instructions about how to access the webinar.
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