In order to distribute a new pharmaceutical product or medical device on the market, all applicable regulatory standards for safety and quality must be met.

Mérieux NutriSciences offers a complete portfolio of GxP-compliant studies and laboratory analyses to ensure the safety and quality of active pharmaceutical ingredients (APIs), excipients, finished products and medical devices.

Our most common tests and services

All our Tests and Services

Mérieux NutriSciences offers a complete portfolio of GxP-compliant studies and laboratory analyses useful for the release of raw materials and finished pharmaceutical products.

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Contamination of pharmaceutical products by microorganisms is a major risk within the pharmaceutical industry, with a potential impact on product integrity and patient safety.

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A medical device, or a material used in a medical device, that comes into direct contact with patients must be able to perform its intended function without inducing significant rejection.

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Mérieux NutriSciences provides a comprehensive range of microbiological services relating to medical devices, to support facility and product monitoring, as well as product development and registration.

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In relation to pharmaceutical products and medical devices derived from raw materials of animal origin, for which the raw material may contain viruses that are dangerous to human health...

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Mérieux NutriSciences performs a wide range of toxicology studies designed to assess the safety of chemicals, pharmaceutical products and excipients.

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The products offered by the medical device sector are subject to various biocompatibility regulations, depending on the intended application and complexity of the device.

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Mérieux NutriSciences has a proven track record in carrying out studies of extractables and leachables in order to detect very low levels of contaminants from materials in contact with medicinal products and medical devices.

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Mérieux NutriSciences offers method development and validation solutions for every analytical challenge, through the availability of several qualified analytical techniques in specialized GMP labs.

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Forced degradation is synonymous with stress testing and plays a key role in the development of stability-indicating and analytical methods, establishing operative conditions and the design of formulations.

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The identification of pharmaceutical impurities is a critical analytical activity in the drug development process. 

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Foreign particles can be a problem in many industries, including the pharmaceutical sector. 

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