How Good Distribution Practice (GDP) is implemented in the Pharma Supply Chain in Asia to drive highly effective Quality Risk Management.
The webinar will look at how the GDP frameworks of international regulators (such as EMA, US FDA, MHRA, ICH, PIC/s) and the technical thought leadership of Industry Associations (such as PDA, ISPE, ISTA) is used to construct and implement a Quality Management System with compliance to international standards and which is used to govern Zuellig Pharma's pharmaceutical, healthcare and medical device operations across 13 countries in Asia. The session will discuss how Zuellig Pharma approaches keeping its QMS current with evolving regulatory, operational and technological change in the industry.
Head of Quality Assurance at Zuellig Pharma
Senior Consultant, Business Development Asia at PDA Asia-Pacific