Are you looking to align your medical devices with the applicable regulatory compliance process?
Obtaining CE marking is mandatory for introducing medical devices on the European market.
For many companies, the process is fraught with uncertainty:
- Is my software considered as a medical device?
- Do I need to carry out a clinical study?
- What are the data protection and cybersecurity requirements?
- What documentation should I prepare?
And so on.
This programme helps you understand the specific characteristics of your product, establish your regulatory roadmap, and, for the most advanced participants, identify accelerators and avoid dead ends in the regulatory processes.
An experienced expert will help you define an action plan for your company and provide additional support to implement the recommendations.