ACI’s European Drug Safety Summit 2018 will be taking place on the 17th & 18th October, London, UK. The two day event will bring together pharmacovigilance personnel from key pharmaceutical companies and will address the challenges in monitoring and maintaining drug safety strategies, will discuss how to apply new technologies and strategic approaches to effectively manage drug safety and will discover key developments in the handling, analysis and reporting of adverse events during trials and understand the regulators requirements with the aim of speeding drugs to market whilst mitigating the risk of recall.
In the Chair:
Monica F. Buchberger (Rusu), Director PV Governance & QPPV, Global Pharmacovigilance Innovation & Development Established Pharmaceuticals, Abbott Laboratories GmbH
Mircea Ciuca, Global Head Medical & Clinical Drug Safety, Vifor Pharma
Marco Sardella, Chief Pharmacovigilance Officer & EU QPPV, ADIENNE Pharma & Biotech
Dr. Paolo Boscani, Deputy EU QPPV & PV Physician, ADIENNE Pharma & Biotech
David J Lewis, Senior Adviser Pharmacovigilance, Novartis
Monika Manske, Associate Director of Global Pharmacovigilance Governance, Mylan Pharmaceuticals ltd
Elizabeth Ursell, Director Pharmocoviglilance, Mapi Group
Ricarda Tiemeyer, Head of Drug Safety & PoC Medical Information, Roche Pharma (Schweiz) AG
Vicky Edwards, QPPV Head of Affilate Vigilance, AbbVie
Lisa Stagi, Drug Safety & Quality Head, Roche S.p.A. Italy
Dominic Bowers, Head of Clinical Operations , Cell and Gene Therapy Catapult.
Saad Shakir, Director, Drug Safety Research Unit
Uwe Gudat, Safety Head, Fresenius Kabi
Lucy Hampshire, Director, Medicines Quality Organisation – Europe, Eli Lilly and Company Limited
Manni Kuthiala, PV Affiliate – Strategic Alliance Manager, Roche
Alison Monckton, Principal Clinical Data Manager, Allergy Therapeutics
Ramón López, Clinical Research Manager, Thrombotargets Europe S.L
If you would like to be considered as a speaker for the event with a 30-45 minute presentation, please submit an abstract for consideration to:
Tel: +44 (0) 20 3141 0611
Attendees will be drawn primarily from pharmaceutical, biotechnology and contract research organisations and include VPs, Directors and Managers/Scientists working in Drug Safety, Pharmacovigilance, Epidemiology, Clinical Research and Development, Clinical Trial Management, Pharmacology, Regulatory Affairs and Compliance, Strategy and Business Development, Risk Management, QPPV
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