To achieve our ongoing assurance to customer fulfillment and confidence, the employees at C.G. Laboratories, Inc. are dedicated to complying with the requirements of ISO 13485:2003 and cGMP-QSR. The culture at our company is built around our NEVER STOP dynamic.
The objective of C.G. Laboratories, Inc. is to offer Service and Guidance.
Celebrating 30 Years of Quality Service in:
Get more with C.G. Laboratories
Completely automated processes are certainly valuable in many circumstances, but what if you need more? Our scientists will work with you, human-to-human, to solve complex issues. We offer customization and comprehensive solutions and will guide you through every step of the process. Tap into our regulatory and scientific expertise. Our goal is to help you succeed. Our service and guidance never stop.
Time is critical when processing complaints. You need your devices processed and returned quickly and efficiently. Our operational TAT performance exceeds our 72-hour objective. Decontamination and sterilization services are customizable for your device specifications. We offer options for data processing and documentation that can be integrated directly with your systems.
Our microbiology laboratory, serving the medical device, tissue and dental industries, can function as your full-time external laboratory or for one-time service needs. We work directly with you to formulate solutions to all of your most challenging problems. Make us your first choice for device testing, microbiological analysis, regulatory testing, environmental monitoring and water testing. Expedited services are available.
We package, sterilize, test, validate and perform shelf-life studies providing an end-to-end solution that gets your device on the market quickly. We will take you from concept through distribution.
MORE ABOUT US
C.G. Labs began life in 1983 as a microbiology laboratory founded by Dr. Glenn Crum. In 1996, we relocated to Granbury, TX and expanded our services to include medical device contract manufacturing. We have grown into a multi-service company with three distinct divisions with 19,000 square feet spanning two sites. All our services are current, regulated and quality-driven. We are registered with the FDA and ISO accredited to 13485:2016 and MDSAP.
Our GET MORE objective gives you great customer service, guidance, quality management and access to experts. We strive to exceed your expectations, to meet government regulations and to make the world a safer place.