Formerly MicroMol (More information about the name change here)
Your platform for classical pharmaceutical microbiology, testing of bacterial cell banks, bacteriophage analytics, pyrogen testing, examination of live biotherapeutic products and genotoxicity- GMP compliant/ISO 17025 accredited … more
Your platform for functional characterization and analysis of your biomolecules combining biochemical, molecular biological, immunological, and cell biological expertise. Ranging from standard techniques, analyzing clinical samples to custom developed bioassays. GMP compliant/ISO 17025 accredited.
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Our platform for biocompatibility testing of medical devices according to ISO 10993 and biological safety of pharmaceuticals, biologicals, and biological active substances using in-vitro based test systems and sensitive testing systemsfor detection of contaminants. GMP-compliant/ISO 17025 accredited
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TentaMedix was founded in 1996 as MicroMol. During the last two decades TentaMedix positioned itself as a reliable analytical service provider: GMP compliant and ISO 17025 accredited
In 2017 TentaMedix joined the TENTAMUS Laboratory Group represented at over 50 locations worldwide. Together with our partners within the Tentamus network TentaMedix can guarantee the highest degree of reliability and quality to its clients.
TentaMedix is your dependable service provider combining our state-of-the-art analytical equipment together with the knowledge and experience of our experts, divided in three main analytical departments.
Our mission is to provide individual support, quick response times, technical expertise combined with the highest quality standards.
We look forward discussing your inquiry and finding the best solution for your needs !
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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Analyst CEO to Join BGN Technologies Patent Committee
Dr. Vivi Ziv, Analyst Research Laboratories’ CEO, has been invited to join BGN Technologies patent committee, as a representative of the biomedical industry. BGN Technologies is the technology transfer company of Ben-Gurion University of the Negev, Israel, which is one of Israel’s leading research universities and among the world leaders in many fields. BGN Technologies,
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