Health products under the DOH-Food and Drug Administration (e.g processed food, food supplements, food additives and ingredients, drugs or medicines, cosmetics, medical and health-related devices, including diagnostic kits and reagents, radiation emitting devices or equipment, household hazardous substances, including urban pesticides, cigarettes, toys and childcare articles, among other products as determined by the DOH-FDA)
New Schedule of Fees and Charges of the Food and Drug Administration for Licensing, Registration and Other Authorizations and Regulatory Services, Amending Administrative Order No. 50 s. 2001, "Revised 2001 Schedule of Fees and Charges for the Corresponding Services Rendered by the Bureau of Food and Drugs". (22 page(s), in English)
Additional guidelines on the FDA services particularly on fees and charges, validity of License to Operate (LTO), Certificate of Product Registration (CPR), Foreign Good Manufacturing Practice Certificate (FGMP), among others.
Provides guidelines on fees and charges on FDA services including those processes/services in issuing licenses and product market authorizations on all health products prior to manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promotion, advertising, or sponsorship.