cGMP processes

CGS is in compliance with cGMP (21CFR – 210 and 211 and the applicable FDA guidelines) standards for services including:

• printing • packaging
• labeling • re-labeling
• R&D sampling • clinical sampling
• warehousing • distribution





Annually, CGS is inspected, on a surprise basis, by the FDA, and for the past 4 years, we have successfully passed this rigorous testing, receiving “no deficiencies or inspectional 483 observations”. CGS is in full compliance and officially in-line with the pharmaceutical industry’s packaging and labeling guidelines. 

CGS offers a complete cGMP production environment, managed and supported by our in-house Quality Assurance Team, our Quality Assurance Director, plus quarterly audits by Jeiven Pharmaceutical Consulting, Inc., a well recognized consulting firm with over 30 years experience in the healthcare and pharmaceutical industries.

What Our Clients Say About Us

"... while printers have many resources at hand, the difference between an average printer and a great one is the extra mile their staff takes to accommodate your every need. This is what CGS has done each time I've worked with them. I recommend CGS without reservation for any of our company's needs."
From a Production Supervisor at a major Pharmaceutical industry creative agency.

cGMP processes inventory management custom online programs warehousing
assembly & kitting quality assurance

CGS Mission Statement

As print goes through another revolution, you and I are faced with changing the way we do business. Over the past year or so, we’ve been adding new technologies, more efficient processes, and a wider selection of products in order to deliver a more complete, one-stop solution for all your communication needs. But I want to assure you now that even with all of these changes, our mission statement remains the same:
To deliver outstanding value, products, and services to you and your organization.


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1200 Ferry Ave.

camden, nj 08104



T 800.575.4238

F 856.486.1466