"Your facility and work ethics are of the highest standards in the world, and I do and have recommended CG Labs to everyone who asks."
Testimonials & Client Feedback
Discover why global medical device OEMs and healthcare manufacturers trust C.G. Laboratories for ISO 13485:2016 certified testing, sterilization validation, and decontamination services.
What Global Medical Device Manufacturers Say About C.G. Laboratories
At C.G. Laboratories, Inc., our service and guidance never stop. Read real operational experiences shared by Quality Assurance Executives, Regulatory Directors, and Supply Chain Leaders across the medical technology industry.
"No task is too small. They make us feel as if I'm their only customer… if they aren't able to provide an answer at the time of the call, they will get with me ASAP."
"Thank you so much for giving me the opportunity to visit CG Labs. Sure, the visit was very informative and helped me a lot! I did not have an idea that your process is so reliable!"
"Thank you again – as an organization C.G. Laboratories has been extremely helpful in getting this validation process started for our team, and the assistance has been much appreciated."
"Y'all do things right the first time. Everyone is professional, knowledgeable, and wonderful to work with throughout the testing program."
"The customer service team is always very helpful in completing technical request forms as well as assisting with documentation tasks that simplify my daily workflow."
"Your team did a great job identifying a mix-up that a hospital sent to your lab. I know how similar our catalog numbers can be, and your attention to detail saved us significant time and risk."
"We don't have in-house EtO capabilities, so having a reliable partner like CG Labs who can get the job done efficiently and accurately is critical for our production schedule."
Built on 40+ Years of Microbiological Integrity
Overseas medical device companies face strict regulatory standards when placing products in international markets. C.G. Laboratories provides technical transparency, rigorous quality management, and responsive communication at every step.
ISO 13485:2016 & MDSAP
Our quality system is audited and certified to rigorous global medical device standards, ensuring full compliance for FDA, EU MDR, and international regulatory filings.
Direct Scientist Access
You speak directly with our senior microbiologists and validation specialists — no customer service barriers or delayed automated response systems.
Consistently Fast Turnaround
Our operational decontamination turnaround time performance routinely satisfies our 72-hour turnaround target, helping clients maintain critical delivery schedules.
Ready to Discuss Your Testing or Validation Project?
Whether you need Ethylene Oxide sterilization validation, bioburden testing, reusable device reprocessing protocols, or contract packaging services, our team of experts is ready to assist you.
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