Already a DIA Member? Sign in. Not a member? Join.

Sign in

Forgot User ID? or Forgot Password?

Not a Member?

Create Account and Join

Holiday Inn Amsterdam - Arena Towers

Nov 06, 2019 8:00 AM - Nov 07, 2019 4:30 PM

Hoogoorddreef 66a, 1101 BE Amsterdam, Netherlands

Global Forum for Qualified Persons for Pharmacovigilance (QPPV)

Networking your path to success amongst a World-class community

Overview

KEEP ME INFORMED

In a changing and expanding world, this is the only forum designed for QPPVs by QPPVs, now in its 13th year and still going strong.

In 2019 the forum is expanding to a global approach on the topics, programme committee composition and programme content. In addition, its location moves to Amsterdam to be in line with the new EMA office.

This Forum continues to identify key trends requiring QPPV awareness, input and oversight. This year’s objectives are built on past successes and have been shaped by valuable feedback provided by participants of the past twelve meetings, plus many years of QPPV and Regulator interaction at this Forum. Moreover, we are looking forward to receive information on the globalization of the QPPV role.

Over time, one of the key successes of the Forum has been the ability to secure the continuing support and involvement of key regulators. Sessions have been open and interactive with attendees appreciating opportunities to raise challenging issues in an informal environment. The 13th QPPV Forum continues this successful approach.

Featured topics

  • The future of pharmacovigilance in the globalisation environment
  • The future of pharmacovigilance in the globalisation environment
  • Global perspective on inspection and audits
  • QPPV oversight and data integrity
  • Signalling and risk management
  • Communication channels for QPPVs
  • EU/Ex-EU QPPV interactions and challenges

Who should attend?

  • Global QPPVs/ Deputies
  • Regulators
  • Pharmacovigilance Consultants
  • Directors of Pharmacovigilance Oversight and Standards
  • Drug Safety Managers/Leaders
  • Auditors
  • Medical and Regulatory Affairs Experts
  • Aspiring PV Specialists/QPPVs

Learning objectives

  • Hear the latest updates and hot topics relating to the role of the QPPV
  • Explore long term PV visions, future directions of the ‘PV world’, and potential impact on the role of the QPPV
  • Network with colleagues and meet regulators
  • Learn from and share experience and ideas with like-minded QPPVs in a neutral environment
  • Better understand regulatory and inspectorate expectations globally
  • Examine current challenges and share potential solutions


KEEP ME INFORMED


Short Course or Primer

To keep you at the forefront.

Nov 05, 2019

Workshop 1:

Introduction to the Role of QPPVs

Nov 05, 2019

Workshop 2:

The PSMF in 2019 - General Developments In - and Outside Europe

Program Committee

  • Peter  De Veene, MD
    Peter De Veene, MD GQPPV
    MSD Belgium, Belgium
  • Elspeth  McIntosh, MBA, RN
    Elspeth McIntosh, MBA, RN Director
    Castle Pharmacovigilance Ltd, United Kingdom
  • Vicki  Edwards, RPh
    Vicki Edwards, RPh Vice President, Pharmacovigilance Excellence and International QPPV
    Abbvie, United Kingdom
  • Mette  Stockner, MD
    Mette Stockner, MD Senior Pharmacovigilance Director
    Savara ApS, Denmark
  • Doris Irene Stenver, MD, MPA
    Doris Irene Stenver, MD, MPA Independent Pharmacovigilance Adviser
    Unique Advice, Denmark
  • Shahinaz  Badr
    Shahinaz Badr Pharmacovigilance Consultant and PVQA Auditor - EMEA
    Pharma Quality Europe, United Arab Emirates
  • Magnus  Ysander, MD
    Magnus Ysander, MD EU & UK QPPV & Head Pharmacovigilance Excellence
    AstraZeneca, Sweden
  • Nicolas  Tsiakkas, MD
    Nicolas Tsiakkas, MD Scientific Director
    NIKOLAS TSIAKKAS AND CO OE, Greece
  • Willemijn  van der Spuij, MSc
    Willemijn van der Spuij, MSc Executive Director, WorldWide Patient Safety International, Europe
    Switzerland
  • Angela  Van Der Salm, PhD, MSc
    Angela Van Der Salm, PhD, MSc Director PV, Managing partner
    DADA Consultancy B.V., Netherlands
  • Gemma  Jimenez Sese
    Gemma Jimenez Sese Senior Director, Deputy EU QPPV
    AstraZeneca, Spain
  • Katarzyna  Swiderek, MPharm, RPh
    Katarzyna Swiderek, MPharm, RPh Director, Safety Evaluation Risk Management (SERM)
    GlaxoSmithKline, Poland

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.