Regulatory Requirements across the Product Development Lifecycle (Part of Biotherapeutics Analytical Summit 2018)

  • 15-16 Mar 2018
  • Sheraton Inner Harbor Hotel, Baltimore, MD, United States

Description

Topics
  • 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

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

Event Categories

Health & Medicine: Pharma
Science: Life Sciences & Biology
Technology: Biotechnology

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