SITE MASTER FILE (SMF)
The Site Master File (SMF) is a crucial document in pharmaceutical manufacturing, providing a comprehensive…
Browsing Tag
Process Validation
5 posts
QUALITY MANUAL
In the pharmaceutical industry, a quality manual is a critical document that describes the company’s entire…
Process Validation Protocol for Aceclofenac, Paracetamol & Serratiopeptidase
Process Validation: Process validation is established documented evidence that provides a high degree of…
PROCESS VALIDATION
Process validation is established documented evidence which provides high degree of assurance that a specific…
PREPARATION AND CONDUCTION OF GMP AUDIT/INSPECTION BY REGULATORY AUTHORITY OR CUSTOMER IN PHARMA
GMP (Good Manufacturing Practice) audits and inspections are critical to assuring pharmaceutical product…