Handbook of Bioequivalence Testing Handbook of Bioequivalence Testing
DRUGS AND THE PHARMACEUTICAL SCIENCES

Handbook of Bioequivalence Testing

    • $59.99
    • $59.99

Descripción editorial

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

GÉNERO
Técnicos y profesionales
PUBLICADO
2014
29 de octubre
IDIOMA
EN
Inglés
EXTENSIÓN
1,007
Páginas
EDITORIAL
CRC Press
VENDEDOR
Taylor & Francis Group
TAMAÑO
9.8
MB
Disposable Bioprocessing Systems Disposable Bioprocessing Systems
2016
Biosimilars and Interchangeable Biologics Biosimilars and Interchangeable Biologics
2025
Biosimilars Development Strategies Biosimilars Development Strategies
2024
Biosimilars and Interchangeable Biologics Biosimilars and Interchangeable Biologics
2016
Handbook of Pharmaceutical Manufacturing Formulations, Third Edition Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
2019
The Future of Pharmaceuticals The Future of Pharmaceuticals
2022
Good Manufacturing Practices for Pharmaceuticals, Seventh Edition Good Manufacturing Practices for Pharmaceuticals, Seventh Edition
2019
Good Design Practices for GMP Pharmaceutical Facilities Good Design Practices for GMP Pharmaceutical Facilities
2016
The Art and Science of Dermal Formulation Development The Art and Science of Dermal Formulation Development
2019
Pharmaceutical Process Validation Pharmaceutical Process Validation
2003
Handbook of Pharmaceutical Granulation Technology Handbook of Pharmaceutical Granulation Technology
2021
The Clinical Research Process in the Pharmaceutical Industry The Clinical Research Process in the Pharmaceutical Industry
2020