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 (like, e.g., Switzerland).
Colleagues who fulfil the QP requirements according
to the EU directive but are
- not (yet) registered, appointed or approved.
- currently not working as QP.
- working in a country outside the EU.
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).
Additional staff members from
regulatory authorities, pharmaceutical organisations or national