What is the purpose of RA 9711?

An Act strengthening and rationalizing the regulatory capacity of the Bureau of Food and drugs (BFAD) by establishing adequate testing laboratories and field offices, upgrading its equipment, augmenting its human resource complement, giving authority to retain its income, renaming it the Food and Drug Administration ( …

What is the purpose of food and drug Act of 2009?

9711 otherwise known as “The Food and Drug Administration Act of 2009”, is mandated to ensure the safety, efficacy or quality of health products which include food, drugs, cosmetics, devices, biologicals, vaccines, in-vitro diagnostic reagents, radiation-emitting devices or equipment, and household/urban hazardous …

What is FDA law?

Food and Drug Administration law, or FDA law, is the body of law that regulates food, cosmetic and drug manufacturing and sale in the United States. The goal of FDA law is to make food and drugs safe for public consumption.

Is Bfad and FDA the same?

The Bureau of Food and Drugs (BFAD) is hereby renamed the Food and Drug Administration (FDA).

What was the purpose of Republic Act no.9711?

republic act no. 9711. an act strengthening and rationalizing the regulatory capacity of the bureau of food and drugs (bfad) by establishing adequate testing laboratories and field offices, upgrading its equipment, augmenting its human resource complement, giving authority to retain its income, renaming it the food and drug administration (fda

How is ASIN law related to R.A 9711?

Also, being covered by special law, it is deemed excluded from the coverage of R.A 9711 and therefore not solely under the jurisdiction of FDA. On the other hand, Section 11 of R.A 8172 gives the Department of Health its rule making power.

How is food defined in R.A 9711?

First, R.A 9711 defines ‘food’ under Section 9, par. e as follows: (e) ‘Food’ means any processed substance which is intended for human consumption and includes drink for man, beverages, chewing gum and any substances which have been used as an ingredient in the manufacture, preparation or treatment of food.

Is the Food and Drug Administration mandated under Republic Act 8172?

Based on the foregoing premises, the Food and Drugs Administration, which is mandated under the Revised Implementing Rules and Regulations of Republic Act no. 8172 to issue a letter or certificate for release for imported salt, is still mandated to do the same prior to release by the Bureau of Customs.

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