cGMP Validation, L.L.C. is one of the largest full service validation/compliance firms in the USA offering services for the finished pharmaceutical, bulk pharmaceutical, biotechnology, medical device, and medical diagnostic industries. cGMP Validation provides companies with integrated compliance solutions that give them the competitive edge in today's demanding and dynamic business environment.

cGMP Validation is staffed with professionals of considerable experience within the pharmaceutical industries and educational disciplines including chemistry, microbiology, engineering, and pharmacy. cGMP Validation has document generation and field execution capabilities including ownership of test equipment required for field execution, as well as in-house procedures necessary to support field execution.

The team has performed over 300 successful project throughout the United States and abroad. Our international experience includes, but is not limited to, projects in Canada, Egypt, Germany, Holland, India, Italy, Korea, Puerto Rico, Sweden and Tunisia. Our clients have been large and small finished and bulk pharmaceutical, biological technology, medical device, and medical diagnostic manufacturers. We have serviced the smallest of companies in the industry, as well as over half of the 20 largest pharmaceutical companies in the world.

Presently, cGMP Validation has offices in Mission, Kansas, Tustin, California, and Metuchen, New Jersey.