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FDA Product Registration

Get your products cleared for the Philippine market.

FDA Product Registration

Overview

Selling food, cosmetics, supplements, medical devices, or drugs in the Philippines requires clearance from the Food and Drug Administration. We guide manufacturers, importers, and distributors through the License to Operate (LTO) and Certificate of Product Registration (CPR) process — preparing technical dossiers, labels, and documentation that meet FDA requirements and reduce the risk of costly delays or rejections.

What’s included

  • License to Operate (LTO) application and renewal
  • Certificate of Product Registration (CPR / CPN)
  • Product classification and labeling review
  • Technical dossier and documentary preparation
  • Liaison and follow-through with the FDA

How it works

  1. 1

    Assessment

    We classify your product and map the exact FDA pathway and requirements.

  2. 2

    Dossier preparation

    We compile formulations, labels, and supporting documents to FDA standards.

  3. 3

    Filing & follow-up

    We submit and actively follow up until your LTO and CPR are issued.

Requirements / documents needed

  • Company registration documents and LTO (if existing)
  • Product formulation / specifications
  • Proposed labels and packaging artwork
  • Certificates from manufacturer (for imported goods)

Frequently asked questions

Yes. A valid License to Operate is a prerequisite before individual products can be registered with the FDA.

Related services

Ready to move forward with fda product registration?

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