By Kim Huynh-Ba, Editor
Published in: Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies and Best Practices
Published on: January 1, 2009
This practical handbook is needed in this area to serve pharmaceutical scientists who handle responsibilities in a variety of functions relating to the drug stability, including R&D, formulation, analytical development, QA/QC, regulatory affairs and production.
Batch Selection • Best Practices • Best Practices • Best Practices • Compliance • Data Analysis • Determination • Extension • Extrapolation • Guidances • Investigations • Methods • Parameters • Planning • Quality • Regulations • Regulatory • Shelf-Life • SOPS • Specifications • Statistics • Study Design • Testing
