Food and Drug Administration

As a regulatory agency under the Department of Health, the Food and Drug Administration, created under Republic Act No. 3720, series of 1963, as amended by Executive Order 175, series of 1987, otherwise known as the “Food, Drugs and Devices, and Cosmetics Act”, and subsequently Republic Act No. 9711 otherwise known as “The Food and Drug Administration Act of 2009”, is mandated to ensure the safety, efficacy or quality of health products as defined by RA No. 97111, which include means food, drugs, cosmetics, devices, biologicals, vaccines, in-vitro diagnostic reagents, radiation-emitting devices or equipment, and household/urban hazardous substances, including pesticides and toys, or consumer products that may have an effect on health which require regulations as determined by the FDA.

License

Other (Open)

Other Access

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License to Operate

List of Licensed Establishments under Food and Drug Administration (FDA)

Dataset Info

These fields are compatible with DCAT, an RDF vocabulary designed to facilitate interoperability between data catalogs published on the Web.
FieldValue
Publisher
Modified Date
2017-10-09
Release Date
2017-06-22
Frequency
Quarterly
Homepage URL
Identifier
a4498113-8378-48ab-bf83-fdd87797f8a4
Coverage
Wednesday, April 29, 2015
License
Other (Open)
Contact Name
Information Communication and Technology Management Division
Contact Email
Public Access Level
Public