ISO 13485 Documentation Overhaul

I need an experienced professional to update my ISO 13485 and FDA 510k documents - this includes Policies and Procedures, Quality Management Systems, and Risk Management Systems. The ideal candidate will have a strong background in ISO 13485 and FDA 510k writing, particularly with these specific sections. The goal is to complete the updates within a month, it's therefore key the freelancer can dedicate sufficient time to this project during this period.