中文|English
What are the documentation preparation requirements for a U.S. Authorized Representative in the medical device registration process?
Category：行业资讯 Date：2024-09-12 17:27:20 Author: Source:
In summary, the AR must prepare and manage a range of documents related to device registration, compliance with FDA regulations, and ongoing communication with the FDA.

For a U.S. Authorized Representative (AR) in the medical device registration process, the documentation preparation requirements typically include:1(2).jpg

  1. Device Registration and Listing: The AR must ensure that the foreign manufacturer’s establishment is registered with the FDA and that each medical device is listed. This involves submitting the FDA’s Form Establishment Registration and Device Listing.

  2. 510(k) Premarket Notification: If applicable, the AR prepares and submits the 510(k) premarket notification to the FDA, demonstrating that the device is substantially equivalent to a legally marketed device.

  3. Premarket Approval (PMA): For high-risk devices requiring premarket approval, the AR assists in the preparation and submission of the PMA application, including detailed data on clinical studies, manufacturing, and labeling.

  4. Labeling Requirements: The AR helps ensure that the device labeling meets FDA requirements, including labeling for user instructions, warnings, and other required information.

  5. Quality System Regulations (QSR): Documentation to demonstrate compliance with FDA’s Quality System Regulations, including manufacturing practices and quality control procedures, must be prepared.

  6. Adverse Event Reporting: The AR must be prepared to manage documentation related to the reporting of adverse events, including any required reports to the FDA.

  7. Registration Updates: Keeping all registration and listing information current, including any changes to the device, manufacturer, or establishment.

  8. Device Specifications and Documentation: Preparing and maintaining comprehensive documentation on the device’s design, performance, and safety specifications.

  9. Regulatory Correspondence: Handling all regulatory correspondence with the FDA, including responses to any inquiries or requests for additional information.

In summary, the AR must prepare and manage a range of documents related to device registration, compliance with FDA regulations, and ongoing communication with the FDA.

Contact Us：

Whatsapp or Wechat：+86 15816864648；email address：hito.lin@grzan.cn


Previous： Can an Authorized Representative provide professional market consulting for your medical device?
Next： Does a medical device Authorized Representative need to understand U.S. regulations and policies?
Back