SITE MASTER FILE (SMF)
The Site Master File (SMF) is a crucial document in pharmaceutical manufacturing, providing a comprehensive…
Browsing Tag
validation
7 posts
QUALITY MANUAL
In the pharmaceutical industry, a quality manual is a critical document that describes the company’s entire…
CLEANING VALIDATION POLICY
Equipment/System/Facility is required to be cleaned post usage of product manufacturing and packaging and…
VALIDATION POLICY
The facility shall be validated in accordance with the systems, guidelines and procedures established by…
Pharmaceutical Definitions
Batch (or lot)
A defined quantity of starting material, packaging material, or product processed in a single…
PROCEDURE FOR PREPARATION OF VALIDATION MASTER PLAN
A Validation Master Plan (VMP) is a document that summarizes an organization's overall philosophy, intentions,…
RESPONSIBILITY OF QA IN PHARMACEUTICAL
Q1: What is the primary role of Quality Assurance in the pharmaceutical industry? A1: The primary…