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Philippine Coast Guard Act of 2009: Repealing RA 5173 2010-02-15: 9994: Amending RA 7432: Expanded Senior Citizens Act of 2010 2010-02-15: 9995: Anti-Photo and Video Voyeurism Act of 2009 2010-02-17: 9996: Mindanao Development Authority (MinDA) Act of 2010 2010-02-18: 9997: National Commission on Muslim Filipinos Act of 2009 2010-02-22: 9998
The Vaporized Nicotine and Non-Nicotine Products Regulation Act, officially recorded as Republic Act No. 11900, is a law in the Philippines which aims to regulate the "importation, sale, packaging, distribution, use and communication of vaporized nicotine and non-nicotine products and novel tobacco products", such as electronic cigarettes and heated tobacco products. [1]
Amending the Philippine National Railways Act or RA 4156: Extending the Life of the PNR: 2014-06-20: 10639: Free Mobile Disaster Alerts Act: 2014-07-15: 10640: Amending the Comprehensive Dangerous Drugs Act or RA 9165: Strengthening the Anti-Drug Campaign: 2014-07-15: 10641: Amending RA 7721: Allowing Full Entry of Foreign Banks: 2014-07-15: ...
DOGE is set to examine multibillion-dollar federal loans to two Tesla rivals. Vivek Ramaswamy said the cost-cutting body would "carefully scrutinize" loans to Stellantis and Rivian.
RA 10645 Member for the Majority An Act providing for the mandatory PhilHealth coverage for all senior citizens, amending for the purpose Republic Act No. 7423, as amended by RA 9994, otherwise known as the "Expanded Senior Citizens Act of 2010" RA 10646 Charter of the Quezon City Development Authority
The New Government Procurement Act of 2024, officially designated as Republic Act No. 12009, is a Philippine law which prescribes the necessary rules to address the lack of transparency and competition in government procurement, eliminate collusion and interference, and lessen the delay in the procurement process by creating the Government Procurement Policy Board (GPPB) and PhilGEPs.
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 ...
Chancellor Chandler held that there was no liability without bad faith. He repeated the In re Caremark International Inc. Derivative Litigation standard of 'utter failure' establishing a lack of good faith, [1] which was approved further in Stone v.