At C.G. Laboratories, we offer a wide range of consultation services aimed at ensuring the safety, quality, and compliance of medical products and devices. With over 40 years of experience, our team of experts is dedicated to providing comprehensive solutions tailored to meet your specific needs.
Tissue Testing
We specialize in tissue testing lab services, offering comprehensive testing methods to ensure the safety and reliability of tissue products. Our laboratory is equipped to handle various tissue testing requirements, including bioburden testing, stability testing, and validation consultations.
Environmental Testing
Our proactive environmental monitoring program provides comprehensive solutions to assure the cleanliness and maintenance of manufacturing facilities. We offer air monitoring, particulate monitoring, surface monitoring, and equipment rental services to meet diverse environmental testing needs.
Sterilization Validation
C.G. Laboratories is a leader in medical device sterilization validation and testing. Our extensive microbiological testing ensures the sterility of devices and compliance with FDA regulations. We provide consulting to help you comply with regulatory requirements and determine the most suitable sterilization method for your device.
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C.G. Laboratories, Inc.
(817) 279-1945
Why Choose CG Laboratories?
C.G. Labs began 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. With C.G. Laboratories, you always GET MORE.
Quarterly Dose Audit
We offer AAMI Quarterly Dose Audits to maintain ongoing compliance and demonstrate continued sterility. Our team provides comprehensive dose audit services to ensure the effectiveness and compliance of the sterilization process.
Endotoxin Testing and Validation
Our services include bacterial endotoxin (LAL) validation using chromogenic methods. We provide thorough testing and validation to ensure the safety and effectiveness of products.
Automated Cleaning
We offer consultation services for automated cleaning and disinfection processes, providing expertise in developing and implementing reliable and efficient cleaning regimens.
Cleanroom Disinfection Validation
Our experts can guide you through the validation of cleanroom disinfection processes, ensuring the effectiveness of disinfection protocols to maintain a sterile environment.
Validation Consultation
Our team of experts is available for consultation on various validation processes, including E-beam dose determination, ethylene oxide sterilization validation, steam sterilization validation, autoclave qualification, and more.
For further inquiries or to request consultation services, please contact C.G. Laboratories during operating hours, Monday to Friday from 8 am to 5 pm.
Sealing Validation
C.G. Laboratories offers sealing validation services to ensure the integrity and reliability of seals, providing comprehensive solutions for sealing validation needs.
Reusable Device Validation
We provide validation services tailored specifically for reusable devices, ensuring the safety and effectiveness of the sterilization process for such products.
Bioburden Testing
Our laboratory conducts thorough bioburden testing, aerobic and anaerobic bacteria testing, and more, to ensure the safety and compliance of medical devices.
Aging and Stability Testing
C.G. Laboratories offers aging and stability study services to assess the quality and stability of products over time, providing valuable insights to maintain product integrity.
