«actively involved with your pharmaceuticals projects.»

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For any requests
and quotation :

gimopharm groupe pharmaceutiquePhone: + 33 (0)1 69 35 54 90
gimopharm groupe pharmaceutiquecontacts@gimopharm.com

Regulatory affairs and scientific drafting

The registration process requires expertise in quality, and evaluation of the efficiency and the risk related to the product.

Our Regulatory Experts write your files, ready for submission to supervisory authorities, and adapted to your particular requirements but also to the concerned type of product: medicines, medical device, cosmetic, dietary supplement.


Medical devices


Dietary supplements