CHMP Meetings

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The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) meets once a month. 

EMA publishes the agendas, minutes and highlights of the CHMP's plenary meetings.

The calendar allows you to find all meeting dates and related documents of the CHMP from 2010. 

November 2017

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  • 2017-11-23 - 2017-11-23 : CHMP

    Joint Biologics Working Party / Quality Working Party workshop with stakeholders in relation to prior knowledge and its use in regulatory applications

    The term ‘prior knowledge’ can refer to both a company’s proprietary knowledge of formulation and manufacturing development of medicinal products and external knowledge from published scientific literature. The use of such prior knowledge to support the development of product formulations, manufacturing processes and control strategies, could be justifiable in certain circumstances. Through a combination of presentations, industry case studies and panel discussions, this joint workshop with regulators and the pharmaceutical industry aims to reach an agreed understanding on what is (and isn’t) considered to be prior knowledge, how can such prior knowledge be used in regulatory submissions, how to justify its use and how to present it in the dossier. EMA will publish a report with conclusions from the workshop. It may also consider further follow-up guidance.

  • 2017-11-06 - 2017-11-09 : CHMP

    Committee for Medicinal Products for Human Use (CHMP): 6-9 November 2017

    The Committee for Medicinal Products for Human Use (CHMP) is the committee that is responsible for preparing the Agency's opinions on all questions concerning human medicines.

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