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Regulatory Affairs

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Lauching a cosmetic product by building a PIF

PIF

The cosmetic formulation has no secret for you but its marketing is still unclear. This article will help you to understand. Indeed, to comply with the regulations and be able to put market cosmetics in Europe, you must develop a

CDMO Expertise 22 October 201911 February 2021 Regulatory Affairs No Comments Read more

ISO 13485 standard: what are the advantages and disadvantages of upgrading to 2016?

In our field, quality is very important. This is why the internationally recognized ISO 13485 standard establishes the requirements for a quality management system specific to the medical device field. In 2016, this standard was reviewed to allow convergence towards

CDMO Expertise 29 June 201811 February 2021 Regulatory Affairs No Comments Read more

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