Granulation, Tabletting and Capsule Technology
11-14 May 2009
Amsterdam, The Netherlands
Who Should Attend
This broadly based course is intended for all scientists and technologists concerned with the development and processing of tablets, capsules and similar products with related drug regulatory affairs.
The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in:
• Quality Assurance
• Marketing
• Validation
• Purchasing
• R&D
• Regulatory Affairs
• Manufacturing/Production
• Engineering Support
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