Summary of the Book
1. Concepts in Validation
2. Documentation
3. Patent Processing and its Applications Form
4. Requirement of GLP, ISO: 9000,WHO and USFDA
5. In Process Quality Control Tests
6. Sampling Plans and Operating Curves
7. Regulatory Controls and Regulatory Drug
Analysis
8. Dosage Forms Evaluation as per I.P.
9. Development of New Analytical Methods
