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The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD / ˈ b iː f æ d /; 1982–2009), is a health regulatory agency under the Department of Health created on 1963 by Republic Act No. 3720, amended on 1987 by Executive Order 175 otherwise known as the "Food, Drugs and Devices, and Cosmetics Act", and subsequently reorganized by Republic Act No ...
The law took effect on June 22, 2002, 15 days after it was signed by Gloria Macapagal Arroyo.Its primary implementing agency is the Philippine Drug Enforcement Agency.The list of illegal drugs may be modified by the DDB through a proceeding initiated by the PDEA, the Department of Health, or any petition by a concerned party.
The regulation of chemicals is the legislative intent of a variety of national laws or international initiatives such as agreements, strategies or conventions.These international initiatives define the policy of further regulations to be implemented locally as well as exposure or emission limits.
The Philippines is a signatory of the United Nations Convention on Narcotic Drugs which lists psilocybin as a Schedule I substance. [36] However, the PDEA has conducted arrests of illegal drug peddlers who also sold psilocybin mushrooms alongside explicitly recognized illegal substances in the past. [37] [38]
The Philippine Drug Enforcement Agency (PDEA, / p iː ˈ d eɪ ə /; [1] Filipino: Ahensiya ng Pilipinas sa Pagpapatupad ng Batas Laban sa Bawal na Gamot [2]) is the lead anti-drug law enforcement agency, responsible for preventing, investigating and combating any dangerous drugs, controlled precursors and essential chemicals within the Philippines.
Regulations Relating to Pollution Control (pollution regulations) Regulations Relating to Restrictions on the Use of Chemicals and Other Products Hazardous to Health and the Environment (product regulations) Svalbard Environmental Protection Act 2001; Waste Regulations (Norway) Water Resources Act 2000; Watercourse Regulation Act 1917; Wildlife ...
Ibogaine is classified as a prohibited substance on the Regulation of the EDI on the lists of narcotics, psychotropic substances, precursors, and auxiliary chemicals. [37] As such, it is subject to the prohibitions stated in the Federal Law on Narcotic Drugs and Psychotropic Substances, which make it illegal to possess, grow, import ...
A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...