In this forum, the expert panel discuss acceptance from regulators on new technology, and other key issues regarding Pharma 4.0.
Technology, Innovation & Impact on the Laboratory
REGISTER TO ATTEND THIS ON-DEMAND EDUCATIONAL EVENT
This latest instalment of PHARMA 4.0: Transforming Pharmaceutical Manufacturing is now available on demand. This eConference and Expert Discussion Forums Series features eminent global thought leaders and covers current and future trends in analytical, process, quality and regulatory issues and their impact on the laboratory of the future and its connection to continuous manufacturing.
PHARMA 4.0: Transforming Pharmaceutical Manufacturing brings together participants from industry, academia and regulatory to create an invaluable resource for recent developments, future trends, challenges and solutions for the development & manufacturing of pharmaceutical & biotechnology products.
Regulatory Challenges
Panellists
Ajaz Hussain
Independent Pharmaceutical Consultant, USA
Sannie Chong
APAC Policy, Roche, Singapore
Lila Feisee
IP Expert, United States Patent and Trademark Office, USA
Ranjit Barshikar
CEO, QbD International, India
Jared Auclair
Global Biotech Professional, Northeastern University, USA
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