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Drug Master File Document Production Product Applications In Europe

4 applications found
In EuropeAvailable In EuropeNear Europe

Separation Equipments for Pharmaceuticals

Separation Equipments for Pharmaceuticals

Our products are present in drug production, where centrifugation is used to convert the raw materials into active substance. E2SE produces efficient equipments for the pharmaceutical industry, in accordance with the required hygiene standards. We provide equipment for pilot productions (testing of raw materials) and industrial productions. ...

ByE.2.S.E.  based in  St-Pierre-lès-Elbeuf, FRANCE


microbiota for Clinical Studies

microbiota for Clinical Studies

Our platform delivers investigational medicinal products that contain diverse and viable communities of donor-derived microorganisms that target multiple functional pathways. We believe that this approach is superior to others being pursued and provides the company with numerous competitive advantages, including: de-risking of clinical programmes based on IMT precedence, accelerated clinical development and opportunities to discover second and third generation products through data generated from clinical ...

ByEnteroBiotix Ltd  based in  Glasgow, UNITED KINGDOM


Intelligent compliance solutions for pharmaceutical industry

Intelligent compliance solutions for pharmaceutical industry

Few industries are regulated as heavily as the pharmaceutical industry. Bringing a new product to market can take years and requires monumental effort. 3E Company stands ready with a comprehensive suite of products and services that can create efficiencies, support product stewardship, mitigate supply chain risk and improve compliance - ultimately shortening the time to get a product on the ...

By3E - SDS and EHS Compliance Data Management Solutions  based in  Carlsbad, CALIFORNIA (USA)


EDXRF spectrometers for pharmaceutical industry

EDXRF spectrometers for pharmaceutical industry

The pharmaceutical industry is one of the most regulated industries. Contaminants in drug products are examined throughout the manufacturing process, since their presence affects drug stability, behaviour and toxicity. Therefore, regulatory bodies such as the European Medicines Agency (EMEA) and the American Food and Drug Administration (FDA) strictly enforce continuous and ongoing analysis of organic or inorganic impurities from raw materials, excipients and Active Pharmaceutical Ingredients (API) through ...

ByXenemetrix Ltd.  based in  Migdal Haemek, ISRAEL

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