News

Latest News | 5 November 2012

Ireland, FDA's Legislative Director, Transitions to new Advisory Role Within Agency

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The US Food and Drug Administration's (FDA) top legislative official, Jeanne Ireland, will leave her current post and assume a new role as senior advisor to Commissioner Margaret Hamburg, the Read More...

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Latest News | 12 October 2012

New Rules to Voluntarily Restrict Prescription Drug and Device Marketing in Ireland

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Pharmaceutical and medical devices industries doing business in Ireland may soon find it more difficult to market their products under new guidance developed by the Irish Medical Council aimed at Read More...

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News Latest News | 31 August 2012

Irish Developer Gets FDA Clearance for Device Uses

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The U.S. Food and Drug Administration has granted clearance of new uses for a gastroenterological system from Ireland.Crospon, based in Galway, Ireland, made the announcement and said the EndoFLIP Read More...

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Latest News | 25 July 2012

FDA Fires Back at Legislative Critics, Blames Manufacturers for Drug Shortages

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The US Food and Drug Administration (FDA) is seeking to distance itself from a June 2012 report by the House Oversight Committee claiming the regulatory agency is the root cause of drug shortages Read More...

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Latest News | 14 May 2012

Irish Medicines Board Announces Transition to Fully Electronic Submission System

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The Irish Medicines Board (IMB) is announcing its adherence to a 2005 agreement between the Heads of Medicines Agencies to transition to a fully electronic system for submitting applications, Read More...

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Regulatory Update | 24 April 2012

Ireland: HIQA Releases Economic Evaluation of Repeat Universal Antenatal Screening for HIV in the Third Trimester of Pregnancy

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A report issued by Ireland's Health Information and Quality Authority (HIQA) contains advice on whether a change in the existing Irish guidelines for the management of human immunodeficiency virus-1 Read More...

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