Search Results for "Method"

US FDA

Category: Guideline | February 26, 2026

1. Facility & Infrastructure Requirements(21 CFR 211.42) Facility Design & LayoutProper separation of operations to avoid mix-ups & contaminationUnidirectional workflow: Personnel →...

Pharmaceutical Change Control

Category: Quality Assurance | February 25, 2026

What is change control A Process which ensures that changes to procedures, materials, methods, equipment, and software are properly documented, approved, validated and traceable. CHANGE CONTROL...

VALIDATION MASTER PLAN (VMP)

Category: Quality Assurance | February 25, 2026

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. ...

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

Category: R&D | February 25, 2026

Title: Raw Material Test Method Material Name: Vitamin E Acetate 50 % Dry PowderGeneric Name            ...

Current Good Manufacturing Practices (cGMP)

Category: Technology | February 23, 2026

Current Good Manufacturing Practices (cGMP) Regulatory Framework for Pharmaceutical Manufacturing Excellence Introduction to cGMP ...

HPLC Method Development

Category: R&D | February 23, 2026

HPLC Method Development Analytical method development is a critical process in pharmaceuticals. The variety of columns, operating parameters, mobile phase compositions, and pH values...

Purified Water Test Procedure

Category: Quality Control | February 23, 2026

TABLE OF CONTENTS Sl. No. Description 01METHOD OF ANALYSIS ...