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Health Laws and Regulation

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Health Law and Regulations
Crystal Sullivan
HCS/545
October 6, 2014
Terry Matherne

Health Law and Regulations
According to "About Hhs" (2014), the purpose of governmental regulatory agencies in healthcare is “for protecting the health of all Americans and providing essential human services, especially for those who are least able to help themselves” (para. 1). Governmental regulatory agencies have taken on the problems of both consumers and health care providers in an attempt to find solutions that will meet everyone’s needs. They take their ideas and the ideas of the public, and create rules and regulations for the healthcare industry.
Regulation plays a critical part in the healthcare industry. The U.S. HHS (the Department of Health and Human Services) has developed several public health regulations to protect the citizens of the United States. The job of the HHS to determine which laws and regulations will be in the best interest of the public. “Through various regulatory bodies, the Department of Health and Human Services (HHS) protects the public from a number of health risks and provides programs for public health and welfare. Together, these regulatory agencies protect and regulate public health at every level” ("Healthcare Regulation", 2014).
The government uses federal regulations to implement public policies. The federal government healthcare agencies are allowed to issue rules during the rulemaking process with the approval of congress. There are several reasons why an agency would want to begin the rulemaking process, and those reasons include: 1. If congress specifically requires a rule or the initiation of a rule. 2. If the agency recognizes a problem or the opportunity to reform a previous rule. 3. If there is an actual petition make by regulated groups or other stakeholders. The public can also petition the agency, but when

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