Detailed description on pharmaceutical cleaning validation on a paper sheet - Hindi.

Validation of Cleaning Programs is now a mandatory requirement under most GFSI food safety standards. Luckily, Safefood 360° has compiled everything you need to know to keep your external auditors more than happy.

A Helpful introduction of computer system validation for beginners.

Validation is a broad concept in the pharmaceutical manufacturing industry. It includes process validation, analytical method validation, equipment validation, cleaning validation and system validation.

ISO 9001:2008 specifies requirements for a quality management system where an organization.

Process validation is establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality characteristics.

World Health Organization, Quality assurance of pharmaceuticals : a compendium of guidelines and related materials. Vol. 2, Good manufacturing practices and inspection

World Health Organization - Quality Assurance of Pharmaceuticals - A Compendium of Guidelines and Related Materials - Volume 1

A quality management system (QMS) is a formalized system that documents processes, procedures, and responsibilities for achieving quality policies and objectives.