GCP-GLP-GMP : Comparison and Understanding of FDA's 3 Major Regulations

For manufacturers for drugs, biologics, biosimilars, generics, and medical devices, firms are subject to various statutory and regulatory requirements under FDA regulations governing Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and current Good Manufacturing Practice (cGMP). To provide safe and effective medical products, it is important for the FDA-regulated industry to accurately understand and apply the applicable regulations and requirements under GLP, GCP and GMP.

Speaker: Dr. David Lim | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details