Latest Advisory

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    FDA Advisory No. 2017-329 || Voluntary Recall of AV-Set B DT INF-E Blood Tubing System with DVR No. 8574 (Article No. AP16641)

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  • FDA Advisory No. 2017-328 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 20)

    FDA Advisory No. 2017-328 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 20)

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  • FDA Advisory No. 2017-327 || CREATION OF A TASK FORCE THAT WILL REVIEW, SUBMIT RECOMMENDATIONS AND TAKE APPROPRIATE ACTIONS RELATING TO THE DENGUE TETRAVALENT VACCINE (LIVE, ATTENUATED), REGISTERED AS DENGVAXIA, AND THE TRANSMITTAL OF APPLICATIONS, LETTER

    FDA Advisory No. 2017-327 || CREATION OF A TASK FORCE THAT WILL REVIEW, SUBMIT RECOMMENDATIONS AND TAKE APPROPRIATE ACTIONS RELATING TO THE DENGUE TETRAVALENT VACCINE (LIVE, ATTENUATED), REGISTERED AS DENGVAXIA, AND THE TRANSMITTAL OF APPLICATIONS, LETTER

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  • FDA Advisory No. 2017-326 || Public Health Warning Against the Purchase and Consumption of the Unregistered Food Product:

    FDA Advisory No. 2017-326 || Public Health Warning Against the Purchase and Consumption of the Unregistered Food Product:

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  • FDA Advisory No. 2017-322 || TERMINATION OF THE VOLUNTARY PRODUCT RECALLOF COBRA DISTAL RADIUS FIXATOR

    FDA Advisory No. 2017-322 || TERMINATION OF THE VOLUNTARY PRODUCT RECALLOF COBRA DISTAL RADIUS FIXATOR

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  • FDA Advisory No. 2017-325 || VOLUNTARY RECALL OF THE NASOPORE STANDARD 8CM NASAL DRESSING WITH PRODUCT REGISTRATION MDR NO. 02341

    FDA Advisory No. 2017-325 || VOLUNTARY RECALL OF THE NASOPORE STANDARD 8CM NASAL DRESSING WITH PRODUCT REGISTRATION MDR NO. 02341

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  • FDA Advisory No. 2017-323 || Public Health Warning Against False, Deceptive and Misleading Health Claims of Pantyliners

    FDA Advisory No. 2017-323 || Public Health Warning Against False, Deceptive and Misleading Health Claims of Pantyliners

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  • FDA Advisory No. 2017-321 || Public Health Warning Against the Purchase and Use of Unregistered Medical Device “Firstaid Blood Lancets”

    FDA Advisory No. 2017-321 || Public Health Warning Against the Purchase and Use of Unregistered Medical Device “Firstaid Blood Lancets”

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  • FDA Advisory No. 2017-320 || Public Health Warning Against the Use of Unregistered Medical Device (Sutures)

    FDA Advisory No. 2017-320 || Public Health Warning Against the Use of Unregistered Medical Device (Sutures)

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  • FDA Advisory No. 2017-324-A || Mga Paalala sa Publiko Ngayong Panahon ng Pasko

    FDA Advisory No. 2017-324-A || Mga Paalala sa Publiko Ngayong Panahon ng Pasko

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  • FDA Advisory No. 2017-324 || Reminders to the Public During the Holiday Season

    FDA Advisory No. 2017-324 || Reminders to the Public During the Holiday Season

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  • FDA Advisory No. 2017-319 || Public Health Warning Against the Purchase and Consumption of Unregistered and Unfortified Flour Products

    FDA Advisory No. 2017-319 || Public Health Warning Against the Purchase and Consumption of Unregistered and Unfortified Flour Products

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  • FDA Advisory No. 2017-316 || Public Health Warning Against the Purchase and Consumption   of the following Unregistered and Unfortified Food Oil  Products:

    FDA Advisory No. 2017-316 || Public Health Warning Against the Purchase and Consumption of the following Unregistered and Unfortified Food Oil Products:

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  • FDA Advisory No. 2017-318 || Suspension of Sale/Marketing/Distribution of Sanofi Pasteur, Inc.’s Tetravalent Vaccine (Live, Attenuated)(Dengvaxia)

    FDA Advisory No. 2017-318 || Suspension of Sale/Marketing/Distribution of Sanofi Pasteur, Inc.’s Tetravalent Vaccine (Live, Attenuated)(Dengvaxia)

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  • FDA Advisory No. 2017-317 || ACCEPTANCE OF ALL APPLICATIONS AT THE FOOD AND DRUG ACTION CENTER (FDAC) CASHIER

    FDA Advisory No. 2017-317 || ACCEPTANCE OF ALL APPLICATIONS AT THE FOOD AND DRUG ACTION CENTER (FDAC) CASHIER

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  • FDA Advisory No. 2017-315 || Voluntary Recall of BD Vacutainer K2 EDTA (K2E) 3.6mg Blood Collection Tube, 13 x 75mm x 2.0mL

    FDA Advisory No. 2017-315 || Voluntary Recall of BD Vacutainer K2 EDTA (K2E) 3.6mg Blood Collection Tube, 13 x 75mm x 2.0mL

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  • FDA Advisory No. 2017-314 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 67)

    FDA Advisory No. 2017-314 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 67)

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  • FDA Advisory No. 2017-313 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 13)

    FDA Advisory No. 2017-313 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 13)

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  • FDA Advisory No. 2017-312 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 12)

    FDA Advisory No. 2017-312 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 12)

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  • FDA Advisory No. 2017-311 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    FDA Advisory No. 2017-311 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

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ANNOUNCEMENT

Application for Registration of Raw Materials and Low Risk Pre-Packaged Processed Food Products

In accordance with FDA Circular No. 2014-0029 entitled "Procedure for the Use of Electronic Registration (E-Registration) System for Raw Materials or Ingredients and Low Risk Pre-packaged Processed Food Products," all low risk food products as listed in Annex A of attached AO2014-0029 and raw materials shall be applied online through electronic registration. Following the said circular, the Public Assistance Information and Receiving (PAIR) Unit shall no longer receive application for the raw materials and low risk food products.

For information and guidance

Attachments:
Download this file (ANNOUNCEMENT.pdf)ANNOUNCEMENT.pdf

Announcement

BAC ADVISORY NO. 2014-002
(ITB No. 14-019)

Construction of FDA Walkway, Waiting Shed, Steel Gate and Perimeter Fence

Subject : Re-Scheduled of PRE-BID CONFERENCE

09 December 2014

The PRE-BID CONFERENCE for the above subject project was not transpired on 08 December 2014 due to TYPHOON RUBY that caused work cancellation of all government offices in the National Capital Region (NCR).

In view thereof, all prospective bidders advised that the PRE-BID CONFERENCE is hereby re-scheduled on 11 December 2014 at 2:00pm, AFO Conference Room

For information and guidance of all concerned.

Procurement and Delivery of One (1) Year Locked in Period and shall be Deemed Renewed until Terminated for Consumable Supply with (50) Units Complimentary Free Use of Printers 4 in 1 Monochrome

SUBJECT : Temporary Suspension of Procurement for ITB 14-017

This is to inform all prospective bidders that the Procurement and Delivery of One (1) Year Locked in Period and Shall be Deemed Renewed until Terminated for Consumables Supply with Fifty (50) Units Complimentary Free Use of Printers 4 in 1 Monochrome (ITB 14-017) is still undergoing review of technical specification and clarification of other requirements thus the aforementioned Project is indefinitely suspended until further notice


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