pharmafileMay 15, 2018
This workshop, through plenary and parallel sessions, will focus on current challenging topics within the global pharmaceutical/biopharmaceutical arena.
Attendees from the different CMC (chemistry, manufacturing and controls) areas will be able to interact with peers from Regulatory Agencies and Industry in sessions enabling interactive cross-functional discussions.
The event will held on 20-21 June 2018 at the Radisson Blu in in Basel, Switzerland.
This program was developed by the CMC Working Group of the DIA Regulatory Affairs Community.
Register as Visitor to CPhI China 2018!
Who should attend?
Professionals involved in:
CMC Regulatory Affairs
CMC Writing
Quality Assurance/Quality Control
Regulatory Compliance
API Development and Manufacturing
Formulation Development and Manufacturing
Analytical Development
CMC Lifecycle Management
CMC Project Management
Learning objectives
Address technical challenges for biological and chemical molecules
Discuss regulatory updates in a globalised environment
Outline regulatory harmonisation initiatives
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