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For effective and efficient public service delivery, the CDRR hereby prescribes the following guidelines for making follow-ups:

  1. Status of applications may checked through the “Doctrack Staus” via FDA website
  2. Follow-ups may be done by submitting Follow-up forms (attached as Annex A) via designated drop box assigned in the Food and Drug Action Center (FDAC). In view of this, the FDAC shall no longer receive follow-up letters from stakeholders.
  3. Follow-up forms may be submitted daily from Monday to Friday, 8:00am to 5:00pm.
  4. No Face-to-face interaction is allowed for follow-ups.

Submission of technical inquiry forms shall be covered in a separate issuance.

This shall take effect immediately are hereby replaced.

Follow-ups Inquiries and Face-to-face interactions