The Department of Trade and Industry Region 3 (DTI-3) is strongly encouraging micro, small, and medium enterprises (MSMEs) engaged in the manufacture and distribution of regulated products—such as food, beverages, cosmetics, food supplements, and household hazardous substances—to secure the necessary licenses and certifications from the Food and Drug Administration (FDA).
“FDA registration is not only a legal requirement; it is a seal of trust for consumers,” said DTI-3 Regional Director Edna D. Dizon. “We strongly urge our MSMEs to undergo FDA registration to ensure their products are safe, properly labeled, and ready for wider distribution,” she added.
The FDA issues both the License to Operate (LTO) for establishments and the Certificate of Product Registration (CPR) for specific products that fall under its regulatory jurisdiction. DTI-3 supports MSMEs in this process by providing technical assistance through its Negosyo Centers and provincial offices, which guide entrepreneurs on compliance requirements, documentation, and product labeling standards.
FDA-regulated products that require licensing include:
- Pre-packaged processed food and beverages
- Food and dietary supplements
- Cosmetics and personal care products
- Household and urban hazardous substances
- Medical devices and over-the-counter medicines/drugs
Many MSMEs are unaware that even online or home-based businesses selling these products are required to register with the FDA to ensure consumer safety and product quality. DTI-3 regularly holds orientations and capacity-building activities to help business owners navigate the registration process and meet FDA standards.
“Complying with FDA requirements can be a game-changer for MSMEs. It signals credibility and enables businesses to join major trade fairs and government-supported market platforms,” added Dizon.
MSMEs interested in FDA registration are advised to visit the nearest Negosyo Center or contact the DTI-3 Regional and Provincial offices for more information and assistance.
