Where Service and Guidance Never Stop
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.
Our ISO 13485 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
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.
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.
The objective of C.G. Laboratories, Inc. is to offer Service and Guidance...
Dr. Glenn Crum, president of C.G. Laboratories, Inc., holds a Bachelors of Science degree from
Texas A&M University and a Masters and Doctorate from the University of North Texas. Before opening
C.G. Laboratories, Inc., Dr. Crum worked with Johnson & Johnson in microbiology research. His work
included microbial research on antimicrobial agents and new product development. Dr. Crum also worked
with cobalt radiation sterilization, microbiology testing, chemistry testing, and ethylene oxide operations.
Dr. Crum founded C.G. Laboratories, Inc. in 1983 with the objective of offering service that meets
customer requirements and provides guidance that exceeds customer expectations. The laboratory offered
medical device testing that included product sterility, pre-sterilized bioburden, environmental monitoring
and sterilization validations. In 1987, Dr. Crum added additional services such as on-site audits for
good manufacturing practices. In 1996, C.G. Laboratories, Inc. was relocated to Granbury, Texas and
expanded its services to include packaging medical devices, sterilization and distribution of medical
devices for various companies worldwide.
Current United States Pharmacopeia is the official pharmacopeia of the United States, published dually with the
National Formulary as the USP-NF. Prescription and over–the–counter medicines and other health care products
sold in the United States are required to follow the standards in the USP-NF. USP also sets standards for food
ingredients and dietary supplements.
American Standard Test Methods, develops and publishes standards detailing international standards and
technical standards for a wide range of materials, products, systems, and services.
Association for the Advancement of Medical Instrumentation, develops and publishes standards detailing the
proper production quality for medical instruments and the procedures in which they are used.
ISO 13485 certification and standards for Medical Device Testing that is an Internationally recognized standard
Publishes standardized, chemical and microbial analysis methods designed to increase confidence in results of
chemical and microbiologic analyses. Government agencies and civil organizations often require that laboratories
use official AOAC methods.
Stability and Aging Temperature and Humidity Standards.
Code of Federal Regulations that deal with Human Tissue and Bone Regulations