Code of Federal Regulations Title 21. Food and Drugs § 21.803.17 What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?

(1) Timely and effective identification, communication, and evaluation of events that may be subject to MDR requirements;

(2) A standardized review process or procedure for determining when an event meets the criteria for reporting under this part;  and

(3) Timely transmission of complete medical device reports to manufacturers or to us, or to both if required.

(1) Information that was evaluated to determine if an event was reportable;

(2) All medical device reports and information submitted to manufacturers and/or us;

(3) Any information that was evaluated for the purpose of preparing the submission of annual reports;  and

(4) Systems that ensure access to information that facilitates timely followup and inspection by us.