PRRC MDR, Medical Device
Budget: €250 – €750 EUR
I'm looking for a professional to be part of my start up team as PRRC( Regulatory affairs specialist) and help me with technical file and ISO13485. The Products are already developed. Producing capacity are cleared allready and the Products are Riskclass 1 nonsterile. So I would appreciate someone with experience in the industry who could provide valuable input and suggestions.
Key Skills and Experience:
- Extensive background in medical device regulations
- Knowledge of healthcare professional needs
- An Swiss or European Person preferred
- Experience in creating and testing device prototypes
Key Skills and Experience:
- Extensive background in medical device regulations
- Knowledge of healthcare professional needs
- An Swiss or European Person preferred
- Experience in creating and testing device prototypes