I will provide eu mdr technical documentation of medical devices

Expert EU MDR Technical Documentation Writer for Medical Devices

Are you looking for a top-notch EU MDR technical documentation writer for your medical devices? Look no further! With my extensive experience in regulatory affairs and technical writing, I can provide you with exceptional service and help you achieve your goals.

I provide following documents,

1. EU Declaration of Conformity
2. Authorized Representative Agreement
3. General Safety and Performance Requirements
4. Material Information
5. Benefit-Risk Analysis and Risk Management
6. Instruction for Use (IFU)
7. Label Specifications
8. Clinical Evaluation Plan
9. Clinical Evaluation & Report
10. Stability and Shelf-life Study
11. Product Catalogue
12. Quality System Procedures
13. List of Products
14. Post Market Surveillance Plan
15. Post Market Surveillance Report
16. Manufacturing Flow Chart
17. Usability Validation Report
18. Bio compatibility Evaluation Report
19. Critical Tests
20. Process Validations

Lets start now;