30 September - 1 October 2015, Workshop, Renaissance Washington, DC, US
30 September - 1 October 2015
Renaissance Washington, DC, US
Through case studies and interactive participation of the attendees, this workshop will explore the barriers for implementation, challenges in adoption of these processes and regulatory changes that may be required through tracks on Continuous Manufacturing and Post Approval Changes.
Organiser: Parenteral Drug Association (PDA)