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.
The HMA works to foster an effective and efficient European medicines regulatory system. It is supported by working groups covering specific areas of responsibility and by the Heads of Medicines Agencies Management Group and Permanent Secretariat.
The European Medicines Agency is a member of the HMA. It works with the other members on these key activities:
- addressing key strategic issues for the European medicines regulatory network, such as the exchange of information and sharing of best practice;
- collectively, being responsible for all areas of medicines regulation, including the mutual-recognition and decentralised procedures;
- focusing on the development, co-ordination and consistency of the European medicines regulatory system;
- supporting the network by providing high-quality professional and scientific resources;
- providing a focus for making the most effective use of scarce resources across the network, such as developing and overseeing arrangements for work-sharing.
EU Network Training Centre (EU NTC)
EMA and HMA have jointly set up the EU Network Training Centre (EU NTC), with the aim of ensuring the exchange of good scientific and regulatory practices across the European medicines regulatory network.
The EU NTC will achieve this by harmonising training standards and offering high quality and relevant training opportunities.
For more information see HMA: EU NTC.
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