Our laboratories are still open and reliably carry out your analyses.
Feel free to use our Live Chat if you have any questions or send your inquiry at office@fdas.org.
Sampling and testing of Active Pharmaceutical Ingredients (API’s) and Excipients is key to ensuring the quality of manufactured product… more
Quality Control testing of each batch of finished product is part of the Batch Release process that gives the patient assurance of a medicinal product over its lifetime… more
Stability Testing evaluates the extent to which a formulated product retains its quality throughout its declared shelf life, … more
Throughout the drug development process and lifecycle analytical test methods are required to support trial data, file submission and post approval batch release… more
Pharmaceutical Microbiology is crucial to the manufacture and production of drugs, biologicals & medical devices. The primary objective is to protect raw materials, the production environment and product from spoilage by microorganisms… more
A Medical Device is any instrument, apparatus, appliance, software, material or other article intended to be used for a medical purpose and must be proven as safe and effective… more
FDAS is an independent contract testing laboratory that has been providing QC analysis to the pharma sector since 2004.
“It is our mission to serve the needs of the pharmaceutical industry for analytical services using flexibility, focus and technical expertise in performing simple or complex analyses. We are driven by quality with total focus on customer satisfaction.”
We offer a comprehensive range of analytical services from our cGMP laboratory in Nottingham.
Because of the “different and difficult” nature of pharmaceutical products it is important to choose a contract laboratory who understand the industry and have the expertise to support your products throughout their lifecycle.
Our expertise and experience of the pharmaceutical sector makes FDAS your lab of choice.
Our testing capabilities are at your service, so why not try us as a new license addition, a backup laboratory, or even to compare what you have in-house. You may save time and money, without compromise and receive a professional, reliable service.
Cannabis Shelf/ Stability Studies
Ensure shelf stability and longevity of your products with a shelf-life study at Columbia Labs! Shelf-life studies have been a staple of food safety in America for decades and are rising as a regulatory requirement across several emerging industries, especially cannabis and hemp-infused products needing to qualify for import, export and consumption. Columbia has
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Canadian-American Contaminants Profiles; The most comprehensive testing on the market.
Regulations vary by region for hemp manufacturers and retailers in the US…Among the many difficulties this poses, this regulatory instability makes it exceedingly difficult to ensure compliance and that proper vendor specifications are met, or to qualify as a vendor for retail. Now you can test hemp ingredients, products, and ancillary ingredients into any regulated
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Kratom Alkaloid Profile Expanded, Validated safety testing
Columbia Laboratories offers reliable, comprehensive contaminant and quality Kratom testing with an 8-business day turnaround time. Kratom Potency Testing Kratom quality, or “potency,” is measured by quantitation of distinct alkaloids. Kratom “potency” testing can be performed on a variety of matrices, from leaf material and extracts to tinctures and gummies. As of 2021, Columbia Labs
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Beta Glucans Testing is now available
Columbia Laboratories now offers quantitative testing for yeast and mushrooms! As the premier consumer safety laboratory in the Pacific Northwest for more than 30 years, Columbia Labs brings rock solid scientific fundamentals to the functional mushroom industry. “We are excited to offer this for our diverse clients who are pushing market doors open with innovative
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Systems and procedure packs
How to pack medical packages Both the MDD 92/43/EEC and the MDR 2017/745 allow packages of different products that are combined in a meaningful context for a specific intended use to be placed on the market. According to the MDD, these must be CE-marked products. The MDR also allows non-CE marked devices if their presence
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Tentamus Group welcomes its first laboratory in Portugal!
Globalab, a laboratory specialized in microbiological analysis for the Environmental and Food industry, becomes the first Tentamus laboratory in Portugal. Based in Marinha Grande (Portugal), Globalab offers a wide range of microbiological analytical services focused on the agri-food and environmental sector. Globalab opened its doors in 2004 and has since become a reference laboratory in the
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