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.
bilacon supports you with the Nutri-Score
Since November, food manufacturers are allowed to use the Nutri-Score voluntarily on their products in order to help consumers to improve their diet. In order for you to be able to create, present and improve the Nutri-Score correctly under food law, bilacon offers a comprehensive support. The international Regulatory Affairs Team supports you in the
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TentaMedix extends its GMP portfolio
Pyrogen testing methods have been successfully inspected by the Regierungspräsidium Tübingen as GMP compliant (Regional Council Tübingen) TentaMedix GmbH is pleased to announce the extension of its GMP relevant testing portfolio. Already in the year 2019, TentaMedix GmbH received the official certificate of recognition from the ZLG and the listing as an officially recognised
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GMP Storage at VelaLabs with 24/7 Call on Duty
January 2021: VelaLabs offers safe and convenient long-term storage of any type of your samples under GMP conditions including also MCBs/ WCBs. The storage of any type of samples such as master cell banks (MCB), working cell banks (WCB), antibodies or small molecules is kept at the highest GMP standard. Furthermore, our on-site storage facility
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Brexit // Where do we go from here?
A cautious agreement has been reached for the future relationship between the European Union and Great Britain. Here are some facts about the given Brexit scenario regarding the pharmaceutical and pharmacy sector: The agreement contains specific provisions for both the pharmaceutical and pharmacy sectors, which are not as comprehensive as hoped: There will be separate
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Megsan Labs Pvt Ltd notified as cGMP Compliant by Health Canada
Megsan Labs is delighted about the receipt of the GMP Compliance Notification from Health Canada. Based on the assessment of the Good Manufacturing Practices (GMP) evidence available for the inspection conducted by U.S. Food and Drug Administration (US FDA) at Megsan Labs from 29 Oct 2019 to 01 Nov 2019, Health Canada has announced that
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VelaLabs Operates State-of-the-art HPLC Systems
January 2021: VelaLabs state-of-the-art high pressure liquid chromatography (HPLC) systems from Agilent and Thermo allow a multitude of different separation techniques. HPLC is an automated high throughput analysis for critical quality attributes of pharmaceuticals. With our optimized analytical HPLC separation techniques such as RPC, IEX, SEC, HILIC, mixed mode, and affinity we offer reproducible detection
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