In 2004 the Heads of Medicines Agencies (HMA) agreed to establish a clinical trials facilitation group (CTFG) to coordinate the implementation of the EU clinical trials directive 2001/20 EC across the member states. The CTFG consists of clinical trials professionals from the EU/EEA Medicines Agencies (NCAs).

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The Heads of Medicines Agencies (HMA) is a network of both the human and veterinary medicines agencies of the European Economic Area. The HMA co-operates with the European Medicines Agency and the European Commission (Directorate-General for Health and Food Safety) in the operation of the European medicines regulatory system. European Medicines Agency EMA and the Heads of Medicines Agencies (HMA) have developed a joint strategy for the next five years that is released for a two-month public consultation today. The draft strategy details how the European medicines agencies’ network can continue to

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Heads of Medicines Agencies | European Medicines Agency The Heads of Medicines Agencies (HMA) is a network of the heads of the ' national competent authorities ', the agencies responsible for the regulation of human and veterinary medicines in the individual countries of the European Economic Area (EEA). The HMA works to foster an effective and efficient European medicines regulatory system.