Powers of Attorney

General information regarding the submission of powers of attorney, including mandatory particulars for individual types of powers of attorney, methods of authentication and sending of powers of attorney, and information on delivery are provided below, in the POWER OF ATTORNEY – General Information 2020 document.

Specimens and procedures relevant to powers of attorney for marketing authorisation activities, pricing and reimbursement regulation, pharmacovigilance, quality defects, good manufacturing and distribution practice are available below, under section Powers of Attorney for the area of marketing authorisations and Pricing and Reimbursement Regulation Section.

Specimens and procedures relevant specifically to powers of attorney for clinical trials on pharmaceuticals are available below, under section Powers of Attorney for clinical trials on pharmaceuticals.