Food Microbiological and physical-chemical control according to quality standard regulations. Food handling analysis. Hygienic-sanitary audits…
Analysis of drinking wáter. Wastewater analysis. Analysis of pool waters. Hemodialysis water testing. Legionella testing…
Microbiological analysis. Stability test. Sterility tests. Challenge test. Official contract required by AEMPS (Spanish Agency of Medicines and Medical Devices)…
Bacterial endotoxins. Sterility tests. Total Aerobic Viable Counts. Testing of Specified microorganisms…
We carry out microbiological and physical-chemical controls of nutritional and dietary supplements according to the current regulations.
Analysis of Biocides and Certificates of Chemical Product. Study of Active Ingredients.
Our laboratory offers analytical services in many sectors and it counts with a broad experience as a technical sanitary consulting (since 1994) in these fields:
We have a wide experience in the sector. Our laboratory operates under the ENAC accreditation (Spanish National Accreditation Body) for over 20 years and we are currently accredited to operate with more than 100 parameters.
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
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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
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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
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