Latest Advisory

  • 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

    Read more

  • 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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  • FDA Advisory No. 2017-310 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    FDA Advisory No. 2017-310 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

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  • FDA Advisory No. 2017-309 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    FDA Advisory No. 2017-309 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

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  • FDA Advisory No. 2017-308 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    FDA Advisory No. 2017-308 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

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  • FDA Advisory No. 2017-307 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 63)

    FDA Advisory No. 2017-307 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 63)

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  • FDA Advisory No. 2017-306 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 11)

    FDA Advisory No. 2017-306 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 11)

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  • FDA Advisory No. 2017-305 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 10)

    FDA Advisory No. 2017-305 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 10)

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  • FDA Advisory No. 2017-304 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 9)

    FDA Advisory No. 2017-304 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 9)

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  • FDA Advisory No. 2017-303 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Supplements Claiming to Contain L-Glutathione:

    FDA Advisory No. 2017-303 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Supplements Claiming to Contain L-Glutathione:

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  • FDA Advisory No. 2017-297 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Products and Food Supplements:

    FDA Advisory No. 2017-297 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Products and Food Supplements:

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  • FDA Advisory No. 2017-299 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 19)

    FDA Advisory No. 2017-299 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 19)

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  • FDA Advisory No. 2017- 296 || Public Health Warning Against the Use of Unnotified Toy and Childcare Article (TCCAs) Products (Batch 11)

    FDA Advisory No. 2017- 296 || Public Health Warning Against the Use of Unnotified Toy and Childcare Article (TCCAs) Products (Batch 11)

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  • FDA Advisory No. 2017-298 || Reiteration of FDA Advisory No. 2017-212 entitled “Public Health Warning Against the Purchase and Use of Unregistered Health Related Device (Water Purification Device) Biocera Alkaline Antioxidant Stick, FDA Advisory No. 2014-

    FDA Advisory No. 2017-298 || Reiteration of FDA Advisory No. 2017-212 entitled “Public Health Warning Against the Purchase and Use of Unregistered Health Related Device (Water Purification Device) Biocera Alkaline Antioxidant Stick, FDA Advisory No. 2014-

    Read more

  • FDA Advisory No. 2017- 301 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    FDA Advisory No. 2017- 301 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    Read more

  • FDA Advisory No. 2017-300 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    FDA Advisory No. 2017-300 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    Read more

  • FDA Advisory No. 2017-295 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 8)

    FDA Advisory No. 2017-295 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 8)

    Read more

List of FDA Electronic Logbook Press Articles

No

Publication

Publication Date

Headline

Link

1

Canadian Inquirer

08/25/2017

FDA launches electronic logbook app

http://www.canadianinquirer.net/2017/08/25/fda-launches-electronic-logbook-app/

2

Diyaryo Pinoy

08/25/2017

Philippine FDA becomes the first in Asia to use mobile app to transform pharmacies

https://issuu.com/diyaryopinoy/docs/diyaryo_pinoy_aug25

3

Pilipino Star Ngayon

08/25/2017

Digital prescription ilulunsad ng FDA

http://www.philstar.com:8080/bansa/2017/08/25/1732470/digital-prescription-ilulunsad-ng-fda

4

Abante-Tonite

08/25/2017

Mobile apps na reseta ipapatupad

http://www.abante-tonite.com/mobile-apps-na-reseta-ipatutupad.htm

5

Philippine News Agency

08/25/2017

FDA launches electronic logbook app

http://www.pna.gov.ph/articles/1007365public-health/347406/

6

Rappler

08/26/2017

FDA to roll out mobile app digitizing logbooks in pharmacies

https://www.rappler.com/nation/180136-fda-electronic-logbook

7

MetroCebu

08/28/2017

FDA launches electronic logbook app

http://metrocebu.com.ph/2017/08/fda-launches-electronic-logbook-app/

8

Manila Times

08/29/2017

FDA e-logbook app expected to modernize public health

http://www.manilatimes.net/fda-e-logbook-app-expected-modernize-public-health/347406/

FDA assures Transparency in Contraceptives Review

The Food and Drugs Administration (FDA) recently assured the public that the evaluation and reevaluation of contraceptives, including those covered by a Supreme Court order, “is aboveboard and transparent”. It also said that the results of the process “will be fully compliant with the standards set by the High Court”.

The assurance was issued by FDA Director-General Nela Charade Puno as the agency nears the completion of the review in line with the certification and recertification of some 50 contraceptives. Several of these contraceptives are covered by an SC order for recertification following a petition by a civic group.

Postponement of the Conduct of Pharmacovigilance Regulations and Guidelines for PV Office Seminar

Please be informed that the conduct of the Pharmacovigilance Regulations and Guidelines for PV Office Seminar on 12-13 October, is POSTPONED and moved to 15-16 November 2017, due to non-availability of resource speakers from the Center for Drug Regulation and Research

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

FDA Circular No. 2017-011 

New Batch Notification Form and Procedure

 

I. RATIONALE

  Pursuant to Section 5 (Reengineering of Systems and Procedures) of Republic Act No. 9485, otherwise known as the Anti-Red Tape Act of 2007, All offices and agencies which provide frontline services are hereby mandated to regularly undertake time and motion studies, undergo evaluation and improvement of their transaction systems and procedures and re-engineer the same if deemed necessary to reduce bureaucratic red tapeand processing time".

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