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.

Customer Satisfaction

  • Guidance

  • Supplier Relationships

  • Product Quality

  • Competitive Pricing

  • Reasonable Lead-time

  • On-Time Delivery

  • Cycle Time Reduction

  • Cost Reduction

Medical Device Laboratory

Prompt, accurate, affordable, and confidential laboratory testing

Medical Device Decontamination

We are experts in developing and validating methods of decontamination for even the most challenging or complex devices.

Contract Packaging

Offering a full service packaging experience from concept to distribution.

Medical Device Laboratory

Prompt, accurate, affordable, and confidential laboratory testing

Medical Device Contamination

We are experts in developing and validating methods of decontamination for even the most challenging or complex devices.

Contract Packaging

Offering a full service packaging experience from concept to distribution.

The objective of C.G. Laboratories, Inc. is to offer Service and Guidance.

Sterilization Validation

Medical Device Laboratory

Our ISO 13485:2016 Certified Laboratory Department is a well-equipped facility with a staff that holds a combined 90+ years of experience servicing the medical device industry. C.G. Laboratories, Inc. is committed to sound scientific principles.

  • Aging Study/Stability Study
  • Biological Indicator
  • Identification
  • Product Sterility
  • Validation
  • Aqueous Biocide
  • Bioburden Testing

  • Environmental

  • Package Integrity

  • Product Testing

  • Water Testing

Medical Device Decontamination

C.G. Laboratories, Inc. has been a leader in the decontamination of medical devices since 1998. We offer decontamination of your medical devices or other products that have been contaminated and potentially exposed to pathogens.

  • Ethlyene Oxide

  • Steam

  • Custom Processes

  • Liquid

  • Gamma Radiation

Contract Packaging

C.G. Laboratories, Inc. offers a wide variety of turn-key contract packaging services to fit your packaging needs. Our services range from sterile medical devices to non-sterile products. Getting your product to market quickly and efficiently.

  • Controlled Packaging areas
  • Sterilization of Product

  • Distribution

  • Large Warehouse

  • Automated Equipment Systems

  • Regulation Testing

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.

DECON
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.

LABORATORY
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.

CONTRACT MANUFACTURING
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.