Determination of the registration procedure best suited to your needs
Evaluation of the technical features and specifications of the medical device.

Coordination of the registration or the renewal of registration
Verification that the product is in conformity with the LPPR specifications.
Management of the compulsory declarations to the relevant authority responsible for monitoring the
technical specifications.
Regulatory monitoring.

Consultation, and follow-up of missions with the relevant authorities
Follow-up of the file after the submission, support, price negociations, discussions.