For companies in the medical device and veterinary device sectors
- Project initiators who wish to study the feasibility and clinical-regulatory impacts upstream, identify the best scenarios to ensure compliance and product commercialisation.
- Manufacturers of medical devices and veterinary devices during the development of their products and in the post-market surveillance phase.
- Service providers, subcontractors, distributors who wish to optimize relations with their customers.
- Organizations wishing to develop best practices for animal health together with consideration of the environmental impact.
Expand on this promising market that improves animal health and welfare.
Prioritize and ensure the integration of regulatory requirements during device life cycle.
Develop clinical solutions applicable in human health and animal health.
Discover our news, case studies and regulatory reflections.