Bioequivalence in Theory & Practice (BTP)

September 10-14, 2011

5 days intensive workshop, under supervision of Prof. Dr. Tasneem Ahmad, Course Director

This seminar was an introduction to Bioequivalence, from starting to end including:

1. Establishment of the CRO for bioequivalence studies

2. Design of the study

3. Conduct of the study

4. Monitoring of the study

5. Regulatory issues in bioequivalence studies

6. Application of good clinical and laboratory practices for bioequivalence studies

7. Documentation from design till reporting

This seminar will polish your information and knowledge, and help you in marketing, export, resolving regulatory issues and therapeutic concerns.

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