Call for independent scientific experts to join EMA’s Pharmacovigilance Risk Assessment Committee (PRAC)

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13/07/2017

Call for independent scientific experts to join EMA’s Pharmacovigilance Risk Assessment Committee (PRAC)

Expressions of interest to be submitted to European Commission by 30 September 2017

The Health and Safety Directorate-General of the European Commission has published a call for expressions of interest to join the European Medicines Agency’s Pharmacovigilance Risk Assessment Committee (PRAC) as independent scientific experts.

This is an opportunity for specialists in pharmacovigilance to be part of one of the most advanced systems for the supervision of medicines and to make sure that medicines for patients in Europe are safe and effective. Appointees can make a real difference to the health of millions of patients in Europe.

This call is intended to select candidates to replace the independent experts currently serving on the Committee. Appointments will be made for a period of three years, which may be prolonged once and thereafter renewed, starting 2 July 2018. The PRAC’s current independent experts may reapply.

Expressions of interest should be submitted to the European Commission no later than 30 September 2017. Interested persons must complete both the application form and the form on declaration of interests, which can be downloaded from the website of the European Commission.

The independent scientific experts will be selected by the European Commission for their expertise. They are expected to attend the meetings of the PRAC, which meets each month, and to contribute to the Committee’s work by actively participating in PRAC’s scientific discussions, examining and commenting on documents. Working for the Committee will also involve some preparatory work before every session.

The PRAC has a key function for the assessment and monitoring of the safety of human medicines. The PRAC’s mandate covers all aspects of the risk management of the use of medicines including the detection, assessment, minimisation and communication relating to the risk of adverse reactions.

The Committee is composed of one member and one alternate appointed by each Member State, six scientific expert members appointed by the European Commission, one member and alternate representing healthcare professionals and one member and alternate representing patient organisations. The six scientific experts are expected to complement and further strengthen the expertise provided by the Member States' appointees and the patient organisations' and healthcare professionals' representatives.

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