Effective Management of Clinical Trial Supply: A European Perspective

Our speaker for the above topic is Mr Matthew Lakelin, Head, Technical Support,
Biotec Services International, United Kingdom. He will be speaking at Pharma & Biotech Supply Chain Asia 2012, part of a series of conferences at the 5th Annual BioPharma Asia Convention 2012, held on 19-22 March at Marina Bay Sands, Singapore.

Mr Lakelin’s career in the Pharmaceutical Industry followed after completing a PhD in respiratory pharmacology. After a number of years working in pre-clinical assessment of respiratory investigational medicinal products he moved into clinical manufacturing and clinical trial distribution. At Biotec he is Head of Technical Support, providing assistance to the company's Operations department.

Mr Lakelin will be exploring more into the following points:

Effective Management of Clinical Trial Supply: A European Perspective
1. Understanding the Qualified Person's (QP) role in EU clinical trials
2. Reviewing key considerations for EU distribution strategies
3. Use of comparators sourced from non-EU territories

If you are keen to find out more, join us at BioPharma Asia Convention 2012 to gain valuable insights from more than 200 experts. Contact us now for more details!

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