The Regulatory Requirements across the Product Development Lifecycle (Part of Biotherapeutics Analytical Summit 2018) covers topics such as:
The Product Development Timeline from IND to Commercialization
The Evolution of Drug Compliance in the US FDA Structure and Function
Good Manufacturing Practice
Good Laboratory Practice
The CMC Section of the Initial IND
Compliance across the Product Development Lifecycle
Meetings with FDA during D
Past Events
Regulatory Requirements across the Product Development Lifecycle (Part of Biotherapeutics Analytical Summit 2018) - 15-16 Mar 2018, Sheraton Inner Harbor Hotel, Baltimore, Maryland, United States (73650)
Important
Please, check "Regulatory Requirements across the Product Development Lifecycle (Part of Biotherapeutics Analytical Summit)" official website for possible changes, before making any traveling arrangements
