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.
LAB obtains ENAC accreditation for the Control of Organic Production Testing Program
ENAC (National Accreditation Entity) opens the year by granting the first accreditations for the “Testing Program for the Control of Ecological Production”. L.A.B (Laboratorio Analítico Bioclínico) is one of the first 3 laboratories that has acquired ENAC accreditation for the organic production control test program in Spain. This is a result of L.A.B demonstrating its
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TentaMedix becomes official testing laboratory for medical devices
Karlsruhe: Animal free biomcompatibility testing of medical devices achieved ZLG recognition – Succesful Re-Accreditation according to ISO 17025:2018 On the 18th of December 2019 the Tentamus company TentaMedix GmbH received the official recognition document and listing by ZLG as testing laboratory according to the guideline 93/42 EWG, 90/385/EWG and DIN ISO/IEC 17025 for biological and
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FDA Issues Final Guidance on Nutrition Facts Label & Serving Size Rules
With the New Year 2020 manufacturers with $10 million or more in annual food sales must comply with FDAs updated Nutrition Facts rules initially announced in May 2016. Since then the rules have been updated and Guidances for Industry have been released by FDA. Rules and Guidance for the Industry can be found here: FDA
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Announcement of Melissopalynology Seminar
Pollen analysis in honey from Argentinia The seminar is intended for experienced melissopalynologists both in the industry and research fields and includes: Lectures providing an overview of honey production, botanical and geographical origins of honey in Argentina Practical morphology part at the microscope, to discuss and learn of the most important pollen grains in
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The entire QSI team would like to thank you for the good and trusting cooperation this year and wish you a Merry Christmas and a successful New Year. We are looking forward to further cooperation in 2020. Your team from QSI Bremen
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Pesticide residues in organic products and their assessment
It seems obvious that no pesticide residues should be detectable in organic products. But even organic products cannot always be completely free of harmful substances. From air and water, for example, pesticides can get into the soil and then into the plants. Pesticides used in the neighbourhood also occasionally drift onto organic fields. Occasionally, organic
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