cGMP Documents for the Pharmaceutical Industry

cGMPs Documents

Available Documentation


Have all of your cGMP documents written by people that are familiar with the Pharmaceutical industry. With Pharma Compliant Documents, LLC, you can rest assured that the work is done by people that knows cGMP requirements as per 21 CFR Parts 210 & 211.

We can provide any cGMP document, including: Batch Records, Analytical Chemistry Test Methods/ Monographs (USP/NF; Ph. Eur; JP; BP, etc.), Equipment and Process Qualification/ Validation, Cleaning Validation,etc. We can provide any cGMP document needed to support the cGMP manufacture of pharmaceuticals.

For additional information about cGMP documentation or the company, contact us

Hours of Operation: Monday - Saturday 7:00 a.m. - 7:00 p.m. • Proudly Serving Customers Worldwide 

About Us

Pharma Compliant Documents, LLC, extends technical writing and cGMP documents for pharmaceutical clients worldwide. Currently, we serve both small pharmaceuticals companies based in the United States and large multinational corporations. 

With more than 20 years of experience in technical writing, we understand the benefits of handling everything electronically. Clients will be able to receive completed documents via e-mail, fax, or scanned copy. If desired, a hard copy can be sent in the mail.

Member of the U.S. Pharmacopoeia Convention