|
|
 |
|
Viewing report
|
|
 |
 |
Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics
Informa Healthcare, Dec 2003, Pages: 704
This text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive approaches for validating analytical methods for pharmaceutical applications.
Customers who bought this item also bought
Handbook of Pharmaceutical Manufacturing Formulations, Second Edition: (Six-Volume Set)
Encyclopedia of Pharmaceutical Technology, Third Edition - 6 Volume Set
ePro - Electronic Solutions for Patient-Reported Data
Cell-Based Assays - Global Strategic Business Report
Personalized Medicine 2010
Molecular Diagnostics - Technologies, Markets and Companies
Sterile Drug Products: Formulation, Packaging, Manufacturing and Quality
Handbook of Pharmaceutical Manufacturing Formulations
Process Validation in Manufacturing of Biopharmaceuticals, Third Edition
Advances in Imaging Biomarkers: Innovative Technologies, Applications in R&D and Clinical Practice, and Informatics and Regulatory Requirements
|
 |
|
|