Medical Devices

Atessia offers tailormade support on a specific project or regulatory activity affecting your medical devices.

  • Listing your essential SOPs
  • Drafting SOPs
  • Quality system maintenance
  • Regulatory validation of materials
  • Submission to the ANSM
  • Implementing the material vigilance case collection system
  • Training your teams
  • Support drafting your contracts
  • Legal advice
  • Regulatory training
  • Declarations of transparency
  • Declarations to professional bodies
  • French and European legislation
  • Atessia Intelligence Service 

Marketing declarations to ANSM

Further information

Download the document "Les dispositifs médicaux"
  • A team of experienced consultants
  • Support tailored to your requirements in project mode
  • Proficiency in regulations
  • A team attuned to new technologies
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Explore other services of Atessia

Pharmacovigilance
Regulatory monitoring
Atessia Master Class
Research & Development Consulting
Post-MA lifecycle management