The client is one of the most renowned and innovative companies in the field of high-end technologies in the segment of adaptive radiotherapy.
Area of expertise
- Post-documentation of validation documents of software and hardware components (embedded systems)
- Validation and documentation under consideration of 62304 and 14971
- Preparation of documents for technical documentation with MDR conformity
We would be happy to provide you with further project references on request. Just let us know what exactly interests you. We will get back to you as soon as possible.
Regulatory Affairs in the field of Labelling
Regulatory approval of class II and III medical devices
segment: medical remanufacturing procedure
Segment: Eye implant