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Current Events

Live Online – Qualified Person Education Course

30 June - 1 July 2021


EQPA Members Area

IMP Working Group Members Area


Document and track your personal development - with the Continuous Professional Development (CPD) Documentation Template

To access the template for documenting and tracking your past and ongoing activities, please go here.

After filling out the form, you will be able to create and print out a PDF file.

Membership Application

Regular Membership:

This membership applies to you if you are either

  • a registered (appointed or approved) QP in a EU member state, official EU member candidate or proposed candidate

or you

Associate Membership:

This membership applies to you if you fulfil the QP requirements according to the EU Directives and you are either

  • preparing to become a QP / working in a EU member state, official EU member candidate or proposed candidate, but you are not (yet) registered, appointed or approved as QP or currently not working as QP

or you

  • are about to assume a similar function (Authorized Person or equal) in a country that has a MRA Agreement with the EU in place (like, e.g., Switzerland)

or you

NOTE: If you are working in a country outside the EU without MRA Agreement in place and/or which is not member of PIC/S, you are unfortunately not eligible for membership in the European QP Association.

Liaison Membership

(Authorities, Inspectorates and Industry Associations only)

One staff member representing a regulatory authority, an inspectorate or an industry association, institution or organisation within or outside the EU (e.g. EMEA, MHRA, BfArM, Swissmedic, EFPIA or VfA).

Guests/Observers

(Authorities, Inspectorates and Industry Associations only)

Additional staff members from regulatory authorities, pharmaceutical organisations or national organisations.