Support Drug Regulation Acts - 932 Words

S.959—Pharmaceutical Compounding Quality, Security and Accountability Act, was introduced into the U.S Senate May 15, 2013 by Thomas Harkin, Democratic senator of Iowa, along with the support of five cosponsors. The bill, if it’d passed would have amended the Federal Food, Drug, and Cosmetic Act (FFDCA) to expand the regulation of compounded drugs. It would have allowed the Federal Government to oversee drug compounders’ operations to ensure drug quality and safety. Most recently, the bill was referred to the Senate Health, Education, Labor, and Pensions Committee but never made it to the floor for a vote. Supporters of S.959 were both Republicans and Democrats. This bill was a bipartisan effort. There was opposition to this bill from the†¦show more content†¦The National Community Pharmacist Association (NCPA) supported the senate’s concern limiting outbreaks like the meningitis outbreak but thought that the compounding section of the bill should be rethought out. They did however agree with the anti-drug counterfeiting portions of the bill. Both the IACP and NCPA were willing to compromise on the bill and were working with the Senate Health, Education, Labor, and Pensions Committee to achieve a compromise. In contrast, the supporters of the bill had quite the opposite to say; arguing that setting national regulation for the drugs would better ensure safety. Each state beforehand had their own regulations and they differed from state to state. With the bill, the compounders would be required to stick to FDA regulations, while still maintaining some authority by overseeing the operations, but then reporting to the FDA. Senator Pat Roberts of Kansas argued the bill was a fair median between federal regulation and state oversight of pharmaceutical processes. Roberts in a statement said â€Å"this legislation protects traditional pharmacy while giving patients more confidence in the quality and safety of their compounded drugs† (as cited by Morris, 2013). Another large supporter was Allan Coukell. He is the senior director for drug and medical devices for the Pew Charitable Trusts. Coukell stated that his group supported the bill and argued it was â€Å"a major advance for theShow M oreRelatedcu1572900 Words   |  4 PagesMedicines Act 1968 The Misuse of Drugs Act 1971 The Misuse of Drugs(Safe Custody) Regulations 1973 SI 1973No 798 as amended By Misuse of Drugs Regulations 2001 The NHS Scotland Pharmaceutical Service (Regulations) 1995 The Social Work (Scotland) Act 1968 as amended by The Regulations of Care Act 2001 The Children Act 1989 The Children s Act (Scotland) 1995 The Data Protection Act 1998 The Care Standards Act 2000 The Regulation of Care (Scotland) Act 2001 The Health and Social Care Act 2001 Read MoreThe Rights And Effectiveness Of Drugs1597 Words   |  7 PagesKefauver–Harris bill that which ensured prescription drug manufacturers to provide proof of the security and effectiveness of drugs before administering them to consumers. 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A substance intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease. A substance (other than food) intended to affect the structure or any function of the body. A substance intended for use as a component of a medicine, but not a device or a component, part or accessory of a device. Biological productsRead MoreDirect Consumer Pharmaceutical Adve rtising ( Dtcpa )1312 Words   |  6 Pagesas â€Å"an effort (usually via popular media) made by a pharmaceutical company to promote ... prescription products directly to patients,† is a common practice and an important issue that impacts the health of U.S. citizens, the prices of prescription drugs and health care, and doctor-patient relationships (Ventola). 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The following is a list of legislation that has a direct impact upon the handling of medicat ion within a social care setting. †¢ The Medicines Act 1968 †¢ The Misuse of Drugs Act 1971 †¢ The Misuse of Drugs (Safe Custody) Regulations 1973 SI 1973 No 798 as amendedRead MoreMODDERN Cures Act and Chronic Disease1524 Words   |  7 PagesShould drug regulation in the United States be significantly revamped in order to encourage development of drugs targeted at chronic disease? In the United States drug regulation is taken very seriously. Congress holds the power to regulate the distribution, manufacture, and use of narcotics. Congress has the power to regulate narcotics through the Bill of Rights. â€Å"Congress may not authorize unreasonable searches and seizures or cruel and unusual punishment of narcotics violators† (Kaplan). 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