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Virtual Event

2025年9月16日 (火) 午後 1:00 - 2025年9月18日 (木) 午後 5:30

(Central Europe Standard Time)

4051 Basel, Switzerland

EU Risk Management Plan Creation

This practical virtual live training course will teach the EU RMP creation skills from both industry and regulatory perspective, including the project management, medical writing, design, and maintenance of the document. It also includes preview of the GVP V Rev 3 and RMP Template Rev 3.

Early-Bird rate for DIA Industry Members Available!

DAYS

HOURS

MINUTES

SECONDS

学部

Representative Invited

Representative Invited

European Medicines Agency

Representative Invited

Representative Invited

European Medicines Agency

Klaudija  Marijanovic Barac, MD

Klaudija Marijanovic Barac, MD

Senior Director, Teva Periodic Reports and Risk Management Centre, Teva, Croatia (Hrvatska)

Klaudija is a physician with more than 20 years of experience in different pharmacovigilance fields. At present, she is Head of TPC – unit responsible for Company Core Safety Information, aggregate reports and risk management worldwide, supporting marketing authorizations and safety strategy for generics, biosimilar and innovative Teva products. Klaudija led in-house development of additional risk minimisation (ARM) implementation tracking tool and ARM digitalisation. Klaudija is Co-Chair of the Pharmacovigilance Working Group in Medicines for Europe.

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