ACT NO. 3740 - ACT TO PENALIZE FRAUDULENT ADVERTISING‚ MISLABELING OR MISBRANDING OF ANY PRODUCT‚ STOCK BOND‚ ETC. Section 1. It shall be unlawful for any person‚ firm or corporation‚ either as principal or agent‚ to display‚ sell‚ barter‚ or exchange‚ or to offer to expose for display‚ sale‚ barter‚ or exchange in the Philippines; or to possess with intent to sell; or to cause to be sent‚ carried‚ or brought for display‚ sale‚ barter‚ or exchange from any foreign country into the Philippines
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drives taking place elsewhere that were arranged by employees representing the University or by official student organizations. In a letter to the campus community‚ Kassing explained that the ban was a result of the U.S. Food and Drug Administration (FDA)’s lifetime blood donor deferral policy for homosexual men. The policy disallows men who have engaged in sexual activity with another man since 1977 from contributing to the blood supply. Following an investigation prompted by concerns about the fairness
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If you were laying on your deathbed and there happened to be a cure for your disease‚ wouldn’t you want to have access to it? Even if the experimental drug was not 100 percent guaranteed to benefit you‚ at least you are giving yourself a chance to survive. On the other hand‚ it can be extremely difficult for clinical trial director’s to get the data that they need‚ without it being rather skewed. Generally‚ a clinical trial would not want to accept a patient who is terminally ill for the fact that
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investigation going on by the U.S. Attorney’s office for the central district of California in collaboration with the FDA (Food and Drug Administration). Outbreak‚ is the word that catches my attention when reading this article. It is a common term used in today’s US/VA history classes. There are outbreaks on political terms‚ accusations perhaps‚ the government society and more. The FDA‚ in this specific case‚ comes in to find out information‚ to solve the problem
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their consumers and people around them‚ also they are destroying public property and public transportation. Because of these deaths and injuries electronic cigarettes must be regulated by the government or else more people will die. Reports from the FDA(Food and Drug Administration) say that they are getting numerous Adverse Event Reports‚ “We regularly receive voluntary reports of Adverse Events involving e-cigarettes from consumers health professionals and concerned members of
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was burning.3 A visible vapor is emitted that disappears within a few seconds. The process of using an e-cigarette is known as “vaping” or “e-smoking.” Quick Facts About E-Cigarettes • Not an FDA-approved tobacco cessation device. • Contain nicotine and detectable levels of known carcinogens and toxic chemicals. • Look very similar to regular cigarettes (especially from a distance). • Manufactured using inconsistent or non-existent quality control processes. Actions for Employers • Determine
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classifications were based on the risk to patients caused by the use of devices device. Congress had given the definitions for the these classes. The regulations that apply to all FDA regulated medical devices are establishing the registration process from manufacturers‚ distributors. Listing of all the devices in right manner as per FDA Meeting the GMP requirements in process of manufacturing Proper labeling Notifying prior to marketing Class I These devices does not require notification before marketing
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Sweden bans bpa in food packaging for under-threes Web. Retrieved from http://www.rsc.org/chemistryworld/News/2012/April/baby-children-food-bpa-ban-sweden.asp Tragger‚ Rebecca. (2012). FDA backs use of BPA in food packaging Web. Retrieved from http://www.rsc.org/chemistryworld/News/2012/April/bisphenol-a-bpa-fda-science-food-packaging.asp
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200 times sweeter than sucrose the accepted standard for sweetness‚ and is also the most dangerous substance on the market that is added to our food. Aspartame accounts for over 75 percent of the adverse reactions to food additives reported to the FDA. There are laws in place that govern the sale of food additives and those laws require that the substances be safe for human consumption. According to research that has been done on Aspartame‚ it may not be completely safe for human consumption and
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regulated by the FDA‚ because e-cigarettes are harmful and can be very dangerous to kids and teenagers. The use of e-cigarettes by teens has doubled since 2011‚ and the electronics devices are being marketed to youths. These devices is putting teens at risk for addiction to nicotine and regular cigarettes. The e-cigarettes are to help smokers to stop smoking‚ but when teens start using e-cigarettes‚ it makes them go on to regular cigarettes. e-cigarettes should be regulated by FDA because it cause
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