Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards.

What is GMP? GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act.

Jun 26, 2025 · The series provides an overview of the regulations pertaining to GMPs and covers topics such as: manufacturing controls, product distribution, plant hygiene, documentation practices, …

Mar 3, 2009 · India Central Drug Standard Control Organization Schedule M - Good Manufacturing Practices and Requirements of Premises, Plant and Equipment For Pharmaceutical Products

The ICH Q7 guideline ensures consistent quality and safety in the production of Active Pharmaceutical Ingredients (APIs) by defining globally recognized Good Manufacturing Practices (GMP) for all …

Good Manufacturing Practices (GMP) for Schedule D Drugs, Part 2, Human Blood and Blood Components Good Manufacturing Practices (GMP) Guidelines Guidance Document - Annex 13 to …

GMP Fundamentals: Eleven-Part Bundle Series Obtain a 10% Savings by Purchasing All Eleven Courses Overview ISPE is presenting an eleven-part series that will focus on the fundamentals of …

Good Automated Manufacturing Practice (GAMP®), is a technical sub-committee of the International Society for Pharmaceutical Engineering (ISPE). The goal of this committee is to promote the …

The GAMP ® Essentials certificate program provides fundamental training on good manufacturing practices (GMPs) for computerized systems in the pharmaceutical and healthcare industries. It …

This course covers areas in which compliance requirements differ most from traditional pharmaceuticals and biologics and will review common deficiencies and problem areas related to the ICH Harmonised …