medical regulations

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April 26, 2014

Published by Medical Blogger at April 26, 2014

What is the MHRA?

MHRA stands for the Medicines and Healthcare Products Regulatory Agency, which is a major force in the healthcare landscape of the United Kingdom. Public health is very import and the MHRA has a big hand in regulating the marketplace as well as steering public health policy. Medicine is always developing and new technologies and medicines are continuously being developed and brought to market. These products are designed to treat many health problems, often in new and innovative ways. All of these products must be thoroughly tested and their quality and safety must be monitored constantly in order to keep the public safe. The Medicines and Healthcare Products Regulatory Agency or MHRA is the government agency that is in charge of all of the extensive testing that is necessary for a new product to be brought to market. The MHRA also controls pharmaceutical compliance as well as medical device compliance in the UK.

November 12, 2013

Published by Medical Blogger at November 12, 2013

What is Medical Compliance?

Medical compliance is the different laws and regulations that the FDA creates in the United States for the health and well-being of the consumer. There are laws and regulations for businesses that work in the food service industry, drug industry, animal care industry, tobacco industry, cosmetic industry, and companies dealing with medical devices and radiation-emitting products. There are even regulations of vaccines, blood, and biological products that are available. Here is some information about how each of these fields gets regulated by the FDA in America to help with compliance in these various areas of business.