In January, the FDA released the second revision of the Draft Guidance, “Current Good Manufacturing Practice—Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act.” The Agency initially submitted the Draft Guidance in 2014 and followed up with Revision One in December 2018. Currently, GMPs for drug
Analytical Chemistry, Microbiology, and
Research & Development Laboratory Services
We have served the Food Ingredients/Flavorings, Cosmetic, Pharmaceutical, OTC, Health and Beauty Care and Dietary Supplement industries since 1966, offering comprehensive microbiology and chemistry product analysis and research and development services.
Registered with the FDA for pharmaceutical testing (Reg. #1527260), cGMP/GLP Compliant and ISO/IEC 17025 Accredited, Q Laboratories can help you maintain the high level of excellence you demand for your products. An independent laboratory, combining state-of-the-art technology with personal service and attention, Q Laboratories can provide services to meet all your testing and quality assurance needs.
For over 50 years, Q Laboratories has maintained excellence in science as well as customer satisfaction, creating a level of confidence and trust among clients that is unparalleled.
Your ultimate goal as a manufacturer is to sell products. The most effective way to sell products is to have the most conclusive, comprehensive information about those products. That is where the Q Laboratories Analytical Chemistry Laboratory comes in, providing the information you need!
Q Laboratories can provide a wide range of Microbiology Laboratory Services. Whether you need a basic enumeration for bacterial presence, screening for specific pathogens, or a computerized microbial identification, our professionals can provide these services for you.
Research & Development Services
At Q Laboratories we understand your laboratory needs do not always follow compendial guidelines or previously determined methodology. We offer versatility in our services in case you need to operate
“outside the box.”
Q Laboratories Blog
After a series of negative reports regarding the cannabidiol (CBD) industry, recent developments have given stakeholders a ray of hope. A December 2019 article on this BLOG discussed the recent Food and Drug Administration (FDA) activities intended to reiterate that CBD is not an approved ingredient for use in foods and dietary supplements,
Title II, Section 202 of the Food Safety Modernization Act (FSMA), signed into law in January 2011, instructed the Food and Drug Administration (FDA) to establish a program for the testing of food by accredited laboratories. FSMA stipulated that accredited labs must possess “a demonstrated capability to conduct one or more sampling and analytical testing