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    Date: 2023-01-25 15:00:45.940774


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    Date: 2023-01-26 08:43:27.394160

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CDRR Product Registration Reference Documents

Requested from DOH by C. Tumpap at 03:00 PM on Jan 25, 2023.
Purpose: Foreign Product Registration
Date of Coverage: 01/25/2023 - 01/25/2023
Tracking no: #DOH-652258500651

Tumpap 03:00 PM, Jan 25, 2023

The document "Revised Guidelines on the Licensing of Veterinary Establishments, Registration and Post-Market Surveillance of Veterinary Drug Products" is available on your website. I just wanted to clarify if this document can already be used as a reference when preparing the required documentation for Product Registration? As this contains more details and more guidelines than the FDA Citizen's Charter CDRR 2022 3rd Edition (e.g. more detailed annexes, etc), is it safe to say that fulfilling all the requirements mentioned in the Revised Guidelines document will cover the Product Registration?

Receiving Officer 08:43 AM, Jan 26, 2023

January 26, 2023

Dear Corelle Maria,

Thank you for your request dated Jan 25, 2023 under Executive Order No. 2 (s. 2016) on Freedom of Information in the Executive Branch, for CDRR Product Registration Reference Documents.

We received your request on Jan 25, 2023 and will respond on or before Feb 15, 2023 03:00:45 PM, in accordance with the Executive Order's implementing rules and regulations.

Should you have any questions regarding your request, kindly contact me using the reply function on the eFOI portal at, for request with ticket number #DOH-652258500651.

Thank you.


FOI Receiving Officer
FOI Officer

Maker 02:15 PM, Jan 26, 2023

Good day!

Please be informed that we have endorsed your request to Food and Drug Administration for action, Kindly await for their response.

Thank you!

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