Quality Assurance

Pharmaceutical CAPA Management Workflow

CAPA Management:

A well-defined CAPA system ensures product safety and regulatory compliance and...

Quality Assurance

Pharmaceutical Change Control

What is change control

A Process which ensures that changes to procedures, materials, methods, equipment,...

Quality Assurance

Pharmaceutical QUALITY MANUAL (QM)

What is QM?

The quality manual is a statement of the Company’s Quality Policy and Quality Objectives of...

Quality Assurance

VALIDATION MASTER PLAN (VMP)

What is VMP

Brief information about Qualification, Validation and calibration of Equipment, Instrument...

Quality Assurance

SITE MASTER FILE (SMF)

What is SMF?

Site Master File is Full information about the site.
Site Master file is a document that...

R&D

Raw Material Test Method - Vitamin E Acetate 50 % Dry Powder

Production

Short Note of Tablet Compression with Defects.

A Quality by Design (QbD) approach to understanding tablet compression failures and preventing them through proper...

Technology

Current Good Manufacturing Practices (cGMP)

Current Good Manufacturing Practices (cGMP) are regulations enforced by the US Food and Drug Administration (FDA) that...