medical device technical document

I am looking for a skilled technical writer to create a regulatory submission document for our finalized medical device. The purpose of the document is for submission to the European Union's Medical Device Regulation (EU MDR). The ideal candidate should have experience in creating technical documents for regulatory submissions and knowledge of EU MDR standards. The document will be used for regulatory purposes and must adhere to the EU MDR guidelines for class 1 medical device ( gel or paste).