Regular Membership:
Registered (appointed or approved) QPs from EU member states,
official EU member candidates and proposed candidates. Similar
functions (Authorized Person or equal) in countries that have a
MRA agreement with the EU in place (e.g. Switzerland) and/or are
members of PIC/S.
Associate Membership:
Colleagues who fulfil the QP requirements according
to the EU directive but are
not (yet) registered, appointed or approved.
working in a country outside the EU.
Liaison Membership:
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:
Additional staff members from
regulatory authorities, pharmaceutical organisations or national
organisations.
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