2016 - Webinar on GCP/GLP/GMP : Comparison and Understanding of FDA's 3 Major Regulations

Description :
Various firms are subject to various relevant and applicable federal regulations including, but not limited to, Good Laboratory Practice (GLP), Current Good Manufacturing Practice (cGMP), and Good Clinical Practice (GCP).
It is important for the industry to accurately understand the requirements under Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and current Good Manufacturing Practice (cGMP).
This seminar is intended to help industry get better familiar with the GLP, GCP and cGMP requirements from regulatory, practical and compliance perspectives.
The speaker will walk you through regulatory and compliance requirements governing GLP, cGMP and GCP.
Areas Covered in the Session :
Applicable Laws and Regulations
FDA Guidance and Standards
Major Misconception
Overview of each regulation ? GCP, GLP, GMP
How each regulation is the same
How each regulation differs
Regulations and Requirements for Good Laboratory Practice
Regulations and Requirements for Good Clinical Practice
Regulations for Current Good Manufacturing Practice
Speaker’s PASS-IT Recommendations: Best Practices
Who Will Benefit:
CEOs
VPs
Compliance Officers
Attorneys
Regulatory Affairs
Clinical Affairs
Quality Assurance
Research & Development
Lab Personnel
Consultants
Contractors/Subcontractors
Anyone who require a general understanding of the FDA’s 3 major regulations