FR.10 Confidentiality and Impartiality Commitment
FR.34 Head of Audit Team/Site Auditor/Product Reviewer/Clinical Specialist Service Agreement
FR.44 Committee Members Confidentiality and Impartiality Agreement
PR.04 Assessment of Complaints and Appeals Procedure
FR.02 Complaint Appeal And Suggestion Form
FR.MED.63 Medical Devices General Terms
Complete MDR Assessment Guideline For Manufacturers
PR.MED.26 Medical Devices Certificate and CE Mark Usage Procedure
FR.MED.51 Change Notification Form
FR.MED.90 (EU) 2017/745 Regulation Product Conformity Assessment Agreement
FR.MED.164 List of Subcontractors
FR.MED.165 List of Standard Fees According to (EU) 2017/745 Regulation
FR.MED.166 MDR Certification Process Flow Chart
FR.MED.176 List of Subsidiaries-Branch Offices
Application Forms
