| Course |
Date |
Venue |
GMP Auditor Training
More information |
4 & 5 November |
London |
How to Audit API Manufacturers
More information |
6 November |
London |
Integrated Tablet Formulation Development
More information |
19 & 20 November 2009 |
London |
Tablet Process Development and Validation and the application of QbD - 2 day course
More information |
23 & 24 November 2009 |
London |
Technology Transfer
More information |
19 & 20 November 2009 |
London |
Stability Testing in Pharmaceutical Development and Manufacturing
More information |
3 & 4 December 2009 |
London |
Analytical Method Development and Validation
More information |
7 & 8 December 2009 |
London |
Supply Chain Management in Biotech/Pharma
More information |
3 & 4 December 2009 |
London |
Pharmaceutical Documentation - a practical approach
More information |
14 & 15 December 2009 |
London |
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Supply Chain Risk Management and Compliance for QP's and RP's
More information |
to be re-scheduled 2010 |
London |
An Integrated Approach to Pharmacokinetics in Drug Development
More information |
to be re-scheduled 2010 |
London |
Introduction to Lean 6 Sigma
More information |
to be re-scheduled 2010 |
|
Validation of Computerised Systems
More information |
to be re-scheduled 2010 |
|
Analytical Chemistry in the Pharmaceutical Industry
More information |
to be re-scheduled 2010 |
|
How are biological entities developed?
More information |
to be re-scheduled 2010 |
London |
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