Handbook of Bioequivalence Testing
-
- $59.99
-
- $59.99
Publisher Description
As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence. In addition, advances in the analytical technology used to detect drug and metabolite levels have m
Good Manufacturing Practices for Pharmaceuticals, Seventh Edition
2019
Good Design Practices for GMP Pharmaceutical Facilities
2016
The Art and Science of Dermal Formulation Development
2019
Pharmaceutical Process Validation
2003
Handbook of Pharmaceutical Granulation Technology
2021
The Clinical Research Process in the Pharmaceutical Industry
2020