Get Qwp-cdrrhr/lrd-02 Annex 05

Filling out the QWP-CDRRHR/LRD-02 Annex 05, the application form for the renewal of registration of medical devices and in vitro diagnostic devices, is an essential process for maintaining compliance. This guide will provide you with detailed instructions to help you complete the form accurately and efficiently.

Follow the steps to complete the form successfully.

1. Select the ‘Get Form’ button to access the application form, which will open the document for your review and completion.
2. Begin filling in your company information in the designated fields, including the name of the medical device, brand name (if applicable), size/product code/reference number, and primary packaging details.
3. Enter the registration number in the field provided. Ensure this information is accurate to avoid processing delays.
4. Compile and attach all required documents as listed in the checklist of requirements for registration, which may include representative samples of your product.
5. Review and confirm your compliance with the current Good Manufacturing Practice guidelines, ensuring all statements made regarding your product are accurate.
6. Sign the form where indicated as a qualified person and the owner or general manager, printing their names, and positions as required.
7. Complete the acknowledgment section, including the required information about the notary public such as their signature and official details.
8. Once all sections are completed, carefully read through your entries to ensure all information is accurate and complete.
9. Save your changes to the completed form, and utilize the options to download, print, or share the document as necessary.

Complete your medical device registration renewal forms online today for a smooth submission process.