Notification Detail

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)
Reference: G/TBT/N/PHL/232

Date of arrival: 2020 March 24     -     Final date for comments: 2020 May 23

Description

: 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.

Objectives

Other

Fields of Activity

Toys
Cosmetics. Toiletries
Pesticides and other agrochemicals
Tobacco, tobacco products and related equipment
Food products in general
Production in the chemical industry
Pharmaceutics in general
Medical equipment

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