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Registry Workshop - Preparing for Future Requirements

Registries are constantly a topic of discussion throughout drug and device development. Challenges exist in terms of ambiguity with structured data collection from existing sources, quality discrepancies, data privacy and data ownership, defining the future of observational data. You know all of this.

How will attending this Registry Meeting make an impact and help YOU overcome these challenges?

This is the only opportunity, to not just listen, but to bring your own views and exchange knowledge, beyond what you can simply read online.

- Discuss best practices with key opinion leaders
- Equip yourself and your teams with the right knowledge and the right tools
- Fine-tune an optimal solution for patient & disease registries
- Define a clear plan for data collection prior to marketing approval
- Prime your organisation for future increases in observational data
- Enhance the functionality and usefulness of data from registries

The EMA hosted the Patient Registries Workshop in 2016 to encourage increased stakeholder collaboration. The DIA Registry Meeting 2017 will build upon on this workshop by providing you with a forum to put collaboration into practice.

Who should attend?
- Associate Directors of Pharmacovigilance and Risk Management
- QPPVs / Deputy QPPVs
- Pharmacovigilance Assessors
- Pharmacovigilance Officers
- Pharmacovigilance Technicians
- Medical Safety Officers
- Senior / Clinical Safety Managers
- Senior / Global / Medical Science Leads
- Compliance Specialists
- Epidemiologists
- Medical Affair Experts
- Risk Management & Business Process -
Management Professionals

Website: https://go.evvnt.com/131263-0

Price
Member Early-Bird: EUR 1230
Industry Member: EUR 1430
Industry Non-Member: EUR 1585
Government/Charitable/Non-profit/Academia (Full-Time) Member: EUR 715
Government/Charitable/Non-profit/Academia (Full-Time) Non-Member: EUR 870

Speakers: Michael Busch-Sorensen Board Member Danish Society for Pharmacoepidemiology Denmark, Maren von Fritschen (PharmD) Managing Partner, Director Regulatory Affairs Addon Pharma GmbH Germany, David Haerry Member of Board of Directors European AIDS Treatment Group Belgium


Event Date: 19 September 2017 - 20 September 2017 Contact Person: Customer Contact Center
Venue: Millennium Chelsea Harbour Hotel, Chelsea Harbour, London, SW10 0XG Email:
Country: United Kingdom Tel: +41612255151

Registration Website: https://go.evvnt.com/131263-1

Submitted by Love Evvnt, Evvnt on Tuesday, 19 September 2017 at 8:00 AM
Category: Health Care & Medical
 
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