What is QM? The quality manual is a statement of the Company’s Quality Policy and Quality Objectives of the organization. Which Guideline follow for preparation of QM? US FDA 21 CFR Parts 210...
What is VMP Brief information about Qualification, Validation and calibration of Equipment, Instrument and System. A document providing information on the company’s validation work programme. ...
Current Good Manufacturing Practices (cGMP) Regulatory Framework for Pharmaceutical Manufacturing Excellence Introduction to cGMP ...
HPLC Method Development Analytical method development is a critical process in pharmaceuticals. The variety of columns, operating parameters, mobile phase compositions, and pH values...
Worst-Case Media Fill Design | Sterile Production ...