FDAS is exhibiting at CPhI 2019 5-7 November 2019, Frankfurt, Germany. Executives from FDAS and all the Tentamus Pharma laboratories will be available throughout the show to discuss any of your pharma testing requirements. Visit us on the Tentamus booth (120F63) and find out how we can help you get your products to market quickly and safely
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.
New regulations on Organic Products in 2020
New regulations for certified flavors in organic products will come into force in the USA in December 2019 and in the EU in January 2020. Food and beverage companies will have to check if the new regulation applies for their products. Use of flavors in organic food & beverage products in the U.S. From
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Testing Pharmaceutical Raw Materials
Any starting material intended for use in the production of medicinal products must be tested for identity, purity and quality. All deliveries of each batch of material must be sampled, tested and the results evaluated prior to manufacturing. As the identity, purity and quality of a complete batch of material is concluded from a small
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Listeria monocytogenes in Food - Challenge Testing
Repeatedly, public recalls of food occur by the qualitative detection of Listeria monocytogenes. The legal basis for these recalls is Regulation (EC) No. 2073/2005 on microbiological criteria for foodstuffs. Chapter 1 lays down food safety criteria for ready-to-eat foods which may favour the reproduction of Listeria monocytogenes and which are not intended for infants or
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Laboratory KUDAM presents its new website
KUDAM Laboratory presents its new corporate online space, which informs you about all its analytical services and the covered industries: Food and Feed, Agriculture and Environment KUDAM Laboratory brings more than 25 years of experience in the field of analytical services and supported many companies in their development. Since 2016, KUDAM is part of the
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New website for Helvic Laboratories in Stoke-on-Trent, UK
Helvic Laboratories, founded in 2010, are a Pharmaceutical Microbiology Laboratory with a difference. Our passion is to offer industry leading Quality and Customer service coupled with very competitive prices. We provide a complete range of microbiological testing services for the Pharmaceutical Industry. Helvic Laboratories – A Tentamus Company, are pleased to announce a new website
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How to ensure the safety of pharmaceuticals?
Impurities in drug products Pharmaceutical manufacturers use materials from a variety of suppliers to compose the final medicinal product for the market. Patient safety is of utmost necessity for these medicinal products. This is ensured by a network of guidelines summarized under the term GMP – good manufacturing practice. Under these GMP guidelines the
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