EXTENSION OF DEADLINE FOR THE SUBMISSION OF COMMENTS FOR THE DRAFT GUIDELINES ON VAPOR PRODUCTS AND HEATED TOBACCO PRODUCTS
This is to inform all concerned stakeholders that the FDA shall be extending the deadline for the submission of comments for the draft guidelines on vapor products and heated tobacco […]
General Guidelines for the Regulation of Vapor Products and Heated Tobacco Products
This is to notify all concerned stakeholders and the general public that the following draft guidelines on the regulation of vapor products and heated tobacco products are now posted in […]
Executive Order No. 106 || PROHIBITING THE MANUFACTURE, DISTRIBUTION, MARKETING AND SALE OF UNREGISTERED AND/OR ADULTERATED ELECTRONIC NICOTINE/NON-NICOTINE DELIVERY SYSTEMS, HEATED TOBACCO PRODUCTS AND OTHER NOVEL TOBACCO PRODUCTS, AMENDING EXECUTIVE ORDER No. 26 (S. 2017)AND FOR OTHER PURPOSES
Please be advised that the following documents are now available online via the FDA website at ww2.fda.gov.ph. Executive Order No. 106 The above law prohibits the manufacture, distribution, marketing, and […]
PRESS RELEASE || FOOD AND DRUG ADMINISTRATION CELEBRATES WORLD NO TOBACCO DAY; LAUDS THE ISSUANCE OF REVENUE REGULATIONS NO. 7-2021
The Food and Drug Administration (FDA) joins the rest of the global community in celebrating World No Tobacco Day with the theme “Commit to Quit”. Each year, on this date, […]
FDA Advisory No. 2019-501 || Gentle reminder for all physicians connected with public hospitals pertaining to DOH-CSC Joint Memorandum Circular 2910-01 and urging them to avoid all interaction with the tobacco/e-cigarette industry
The Food and Drug Administration (FDA) informs heads of hospitals that e-cigarette companies are currently engaging physicians, from both the public and private sector, in an attempt to recruit them […]
Information, Education and Communication (IEC)-CCHUHSRR
Downloadables Information, Education and Communication (IEC) Center for Cosmetics and Household Urban and Hazardous Substances Regulation and Research (CCHUHSRR) ● Consumer Protection TOY Safety 101: “Fun in the Sun: Choosing […]
FDA Advisory No.2023-0461 || Discontinuation of the Issuance of FDA Authorizations, Including License to Operate (LTO) and FDA Product Batch Declaration Certification
The Food and Drug Administration (FDA) informs all concerned stakeholders of the discontinuation of the issuance of the license to operate (LTO) and the product batch declaration (PBD) certification for […]
Downloadables 2
Downloadables Public Assistance Information and Receiving Integrated Application Forms and Process In pursuant to FDA Circular No. 2014-003: Filing and Receiving of Registration, Licensing and Other Applications Using the Integrated Application Form, […]
Draft for Comments || Amendment to Administrative Order No. 2020-0017 entitled, “Revised Guidelines on the Unified Licensing Requirements and Procedures of the Food and Drug Administration Repealing Administrative Order No. 2016-0003”
All comments may be sent at [email protected]. The deadline for submission of comments is on 14 October 2022. I. RATIONALE Republic Act (RA) No. 9711, otherwise known as the “Food […]
FDA Press Statement || The Food and Drug Administration (FDA) joins the Department of Health (DOH) in requesting the Presidential veto of Senate Bill No. 2239 and House Bill No. 9007, or the Vape Bill. The FDA strongly echoes the sentiments of the DOH that the Vape Bill is not a health bill.
The Food and Drug Administration (FDA) joins the Department of Health (DOH) in requesting the Presidential veto of Senate Bill No. 2239 and House Bill No. 9007, or the Vape […]