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.
Analyst GMP Certification Extension
The Israeli MoH notified Analyst Research Laboratories that it has successfully passed its latest audit and has been rewarded with an extension of its GMP certification. The Israeli Institute for Standardization and Control of Pharmaceuticals operating under the Israeli MoH, is recognized by the European Commission under the Agreement on Conformity Assessment and Acceptance of
... Continued
Tentamus Pharma Group at CPhI worldwide 2021
The Tentamus Pharma Group bundles all competences in the field of drug and medical device testing and is made up of class leading independent laboratories, providing high quality service and support to our clients worldwide. Our client base ranges from small start-up companies to multi-national corporations, encompassing a comprehensive and diverse portfolio of services to
... Continued
More time to be ready for IVDR?
About 90 % of all in vitro diagnostic (IVD) manufacturer cannot benefit from transition period laid down in Article 110 of Regulation (EU) 2017/746 (IVDR) and must be ready for IVDR in May 2022. The new Regulation will replace the current Directive 98/79/EC on in vitro diagnostic medical devices from 26 May 2022. The main
... Continued
VELTIA Labs for Life Cyprus has updated its Scope of Accreditation!
“Your life’s quality, our top priority” – VELTIA Cyprus is committed to VELTIA LABS FOR LIFE’s motto and has set a clear target for 2021. The goal was to upgrade its nutritional lab and provide its clients the services of one “stop-care lab”. “After a successful 4-day-audit conducted by CYS-CYSAB (Cyprus Accreditation Body) we are
... Continued
Foundation of Tentamus Pharma & Med Deutschland GmbH
Formation of a new company out of BLS-Analytik GmbH, TentaMedix GmbH and DSIpharm Oldenburg The Tentamus Group pleased to inform you that BLS Analytik GmbH, TentaMedix GmbH and DSIpharm Oldenburg have merged as one company with immediate effect as Tentamus Pharma & Med Deutschland GmbH. The company’s headquarters are located in Bad Kissingen, Columbiastraße 14
... Continued
Laboratorio Control extends its ENAC scope in Feed, Food and Food Additives
Committed to the continuous improvement of its analytical services, Laboratorio Control extends its ENAC (National Accreditation Body) accreditation in the Food and Animal Nutrition sectors. The Molecular Biology Department of the laboratory has successfully passed the ENAC audit which focused on the evaluation of the analytical method for the detection of Salmonella spp. and
... Continued
