I will write regulatory documents for medical devices

I will provide medical device regulatory documents which will comply with all the regulations laid out by the EU or FDA. I will also revise an existing medical document or report as per the criteria if the device's intended purpose has been changed. Moreover, I will also write and summarize the biological and clinical evaluation reports (a prerequisite of the medical device regulations - MDR ) of your given device. I will use the following sources (but not limited to) for skimming through the published literature on related medical devices:

1. PubMed
2. Google Scholar
3. Cochrane library

I can also write a risk analysis or MDR reporting document according to the MDR regulation of your jurisdiction.