Heads Of Medicines Agencies
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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 European Economic Area (EEA) was established via the ''Agreement on the European Economic Area'', an international agreement which enables the extension of the European Union's single market to member states of the European Free Trade Ass ...
. The HMA co-operates with the
European Medicines Agency The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or Euro ...
and the
European Commission The European Commission (EC) is the executive of the European Union (EU). It operates as a cabinet government, with 27 members of the Commission (informally known as "Commissioners") headed by a President. It includes an administrative body o ...
(
Directorate-General for Health and Food Safety The Directorate-General for Health and Food Safety (DG SANTE), until 2014 known as the Directorate-General for Health and Consumers (DG SANCO), is a directorate-general of the European Commission. The DG is responsible for the implementation of E ...
) in the operation of the European medicines regulatory system. The network provides a forum for the co-ordination and the exchange of views and proposals on issues concerning the European regulatory system and the role of the national authorities within that system. The HMA, initially known as the Heads of Agencies, was established in 1995 with a first full meeting taking place in Amsterdam in February 1996. Initially the network comprised only agencies responsible for the regulation of medicines for human use. In February 1998, a parallel group bringing together the heads of agencies responsible for medicines for veterinary use held its first meeting. The two groups started organising joint meetings in 2000 and since 2004 these activities have been integrated under the umbrella of the HMA.


Membership

The HMA comprises 46 national competent authorities responsible for the regulation of human and/or veterinary medicines. These 46 national authorities represent the 28 EU member states as well as the three additional European Economic Area members, Iceland, Liechtenstein and Norway. Of the 46 NCAs, 15 have responsibility only for human medicines; 14 are purely veterinary agencies; 17 are joint veterinary and human agencies; and some veterinary agencies are integrated with their respective national food safety agencies or respective ministries. Some have responsibility for pricing and reimbursement of human medicines. 22 have joint responsibility for medicines and medical devices. All are accountable to their national governments. Together with the European Medicines Agency and the European Commission, these national authorities form the European medicines regulatory system.


Main activities

Medicines can be authorised in Europe through a number of ways: * The
centralised procedure Centralisation or centralization (see spelling differences) is the process by which the activities of an organisation, particularly those regarding planning and decision-making, framing strategy and policies become concentrated within a particu ...
, which is the responsibility of the
European Medicines Agency The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or Euro ...
* National procedures, which are the responsibility of the national authority of each country * Non-centralised procedures, co-ordinated by the HMA: ** The decentralised procedure ** Mutual-recognition procedures. The initial focus of the network in 1995 was the operation of a Mutual Recognition Facilitation Group which was given full legal status in 2003 as the HMA mandated Co-ordination Group for Mutual Recognition and Decentralised Procedures (CMD). In 2012, new European pharmacovigilance legislation added to the role and decision-making powers of the CMD in respect of human medicines. Over the years, the HMA has added to its coordination activities to include
clinical trials Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietar ...
authorisation, worksharing of safety aspects, pediatric indications, interpretation of legal provisions and product testing. It has also established a number of shared initiatives across the network which has resulted in Europe-wide projects concerning IT infrastructure, benchmarking, training programs and communication policy. These projects are intended to bring efficiencies and greater consistency to the European medicines regulatory system.


Operations

The HMA is based on a model of cooperation and worksharing across statutory as well as voluntary regulatory activities. The network does not have a permanent executive or head office. However a HMA member agency is requested to support the network by providing professional and scientific resources. The Management Group, consisting of a number of national heads, co-ordinates and facilitates the operation of the HMA and also supervises the work of the HMA Permanent Secretariat. The HMA PS facilitates and supports the work of the HMA, the HMA MG and the EU presidency by ensuring co-ordination, consistency and continuity of their work and activities and providing the collective memory of HMA. After the finalisation of a joint HMA/EMA strategy to 2020, in February 2016 the HMA adopted a Multi Annual Work Plan to bring the joint overarching strategy into operation on the HMA level with the involvement of all National Competent Authorities.


References


External links

{{authority control 1995 establishments in the European Union Agencies of the European Union Health and the European Union