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COVID19 UPDATES
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COVID19-related Updates

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Latest Advisories

FDA Advisory No.2022-1081-A || Babala sa Publiko tungkol sa Paggamit ng mga sumusunod na Beripikadong Pekeng Gamot na:

Pinapayuhan ng Food and Drug Administration (FDA) ang publiko laban sa pagbili at paggamit ng mga sumusunod na beripikadong pekeng...
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FDA Advisory No.2022-1078 || Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “AA MEDICAL+HEALTHCARE NASAL OXYGEN CANNULA”

The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the...
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FDA Advisory No.2022-1077 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “READING GLASSES”

The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the...
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FDA Advisory No.2022-1076 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “MEDIPACK® GAUZE PADS (4” X 4” X 12 PLY 24 X 28 MESH)”

The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the...
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FDA Advisory No.2022-1080-A || Babala sa Publiko tungkol sa Pagbili at Paggamit ng Beripikadong Pekeng Gamot na “Mefenamic Acid (Ponstan®) 500 mg Tablet”

Pinapayuhan ng Food and Drug Administration (FDA) ang publiko laban sa pagbili at paggamit ng sumusunod na beripikadong pekeng gamot:...
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FDA Advisory No.2022-1080 || Public Health Warning Against the Purchase and Use of the Verified Counterfeit Drug Product “Mefenamic Acid (Ponstan®) 500 mg Tablet”

The Food and Drug Administration (FDA) advises the public against the purchase and use of the counterfeit version of the...
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FDA Advisory No.2022-1081 || Public Health Warning Against the Purchase and Use of the following Verified Counterfeit Drug Products:

The Food and Drug Administration (FDA) advises the public against the purchase and use of the counterfeit version of the...
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FDA Advisory No.2022-1072 || INTERIM PROCESS FOR INTENDED LICENSE TO OPERATE VARIATION APPLICATIONS FOR VAPOR PRODUC T AND HEATED TOBACCO PRODUCT ESTABLISHMENTS

In accordance with the implementation of Administrative Order No. 2020-0055 entitled “Regulation  on Vapor Products and Heated Tobacco Products (HTPs)...
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FDA Advisory No.2022-1071 || REITERATION ON THE PROCESSING OF LICENSE TO OPERATE (LTO) APPLICATION FOR VAPOR PRODUCT AND HEATED TOBACCO PRODUCT ESTABLISHMENTS

The Food and Drug Administration (FDA) would like to inform all concerned stakeholders that the requirement for a license to...
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Announcement

VENUE FOR UNIFIED LICENSING SEMINAR  (ULS –RV) ON 19-20  JUNE 2019
Please be informed that the venue of the Unified Licensing Seminar (ULS – RV) on 19-20 June 2019 will be ...
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VENUE FOR CENTER FOR DRUG REGULATION AND RESEARCH QPIRA SEMINAR (QCDRR – NCR) ON 13-14 JUNE 2019
Please be informed that the venue for the Center for Drug Regulation and Research QPIRA Seminar (QCDRR-NCR) on 13-14 June ...
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