Irish Medicines Board
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Irish Medicines Board
The Health Products Regulatory Authority is an Irish regulatory agency. It advises the Irish government. It is responsible for both public and animal health. It regulates medicines, medical devices, clinical trials and other health products and monitors the safety of cosmetics. Until July 2014 it was known as the Irish Medicines Board. The Irish Medicines Board suspended Nimesulide from the Irish market and referred it to the EU Committee for Human Medicinal Products for a review of its benefit/risk profile due to the reporting of six cases of potentially-related liver failures by the National Liver Transplant Unit at St. Vincent's University Hospital between 1999 and 2006. In July 2018 the authority recalled a number of medicines containing the active ingredient Valsartan when an impurity was identified in a valsartan active substance manufactured at a facility in China. It produced a report on medicinal cannabis in 2018 which suggested a controlled access programme for ca ...
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Regulatory Agency
A regulatory agency (regulatory body, regulator) or independent agency (independent regulatory agency) is a government authority that is responsible for exercising autonomous dominion over some area of human activity in a licensing and regulating capacity. These are customarily set up to strengthen safety and standards, and/or to protect consumers in markets where there is a lack of effective competition. Examples of regulatory agencies that enforce standards include the Food and Drug Administration in the United States and the Medicines and Healthcare products Regulatory Agency in the United Kingdom; and, in the case of economic regulation, the Office of Gas and Electricity Markets and the Telecom Regulatory Authority in India. Legislative basis Regulatory agencies are generally a part of the executive branch of the government and have statutory authority to perform their functions with oversight from the legislative branch. Their actions are often open to legal review. ...
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