Webinar on GCP/GLP/GMP : Comparison of FDA’s 3 Major Regulations

These are the 3 major regulations FDA uses to regulate the Pharmaceutical/Medical Device industries in the USA. This web presentation presents an overview of FDA’s 3 major regulations – Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Although varying slightly in different regions of the world these 3 regulations have the same basic elements and interpretations globally. Learn the requirements for each regulation, how they fit into the development process and how they are same and how they differ. Learn when to use each regulation and how FDA interprets the regulation.

Areas Covered in the Session :

• Overview of each regulation – GCP, GLP, GMP
• How each regulation is the same
• How each regulation differs
• FDA’s interpretation of each regulation

Who Will Benefit:

• Regulatory Affairs Personnel
• Research Personnel
• Manufacturing Personnel
• Clinical Personnel
• Nonclinical Personnel
• Lab Personnel
• Quality Personnel
• Auditors
• Personnel who require a general understanding of the FDA’s 3 major regulations

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299