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The European Drug Safety Summit 2018

Date: 17th October 2018 - 18th October 2018 Location: London - UK

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.

Topics Include:

  • Meeting Safety Requirement: Regulator’s Perspective
  • Building a Pharmacovigilance Strategy
  • Evolving PV Strategies for Tomorrow
  • Technological Advancement in Pharmacovigilance
  • Clinical Data Management
  • The Role of Big Data and Social Media in PV
  • Ensure Drug Safety & Risk Minimisation Measures
  • Latest Development & Innovation Approach for Effective Signal Management
  • Development of Qualified Personal Responsible for Pharmacovigilance (QPPV)
  • Pharmacovigilance for Advanced Therapies


17th October 2018
18th October 2018
Event Category:


Timothy Rowley-Evans – Delegate Sales
+44 20 3141 0614
Cheryl Williams – Marketing, Sales & Media Partnerships
+44 (0) 203 141 0623
Joshua Hill – Sponsorship
+44 (0)20 3141 0610
Mikhail Kryukov – Content
+44 (0) 20 3141 0649
Jayme Burns – Logistics
+44 (0) 203 141 0640


We will confirm the venue approximately 4-6 weeks before the event to ensure we find the most suitable space because numbers can vary dramatically. There will be a discounted accommodation rate for conference attendees.
London, United Kingdom
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  • Meeting Safety Requirement: Regulator’s Perspective
  • Building a Pharmacovigilance Strategy
  • Evolving PV Strategies for Tomorrow
  • Technological Advancement in Pharmacovigilance
  • Clinical Data Management
  • The Role of Big Data and Social Media in PV
  • Ensure Drug Safety & Risk Minimisation Measures
  • Latest Development & Innovation Approach for Effective Signal Management
  • Development of Qualified Personal Responsible for Pharmacovigilance (QPPV)
  • Pharmacovigilance for Advanced Therapies

Confirmed Speakers:

Mircea CiucaGlobal Head Medical & Clinical Drug Safety, Vifor Pharma

Marco Sardella, Chief Pharmacovigilance Officer & EU QPPVADIENNE Pharma & Biotech

Dr. Paolo Boscani, Deputy EU QPPV & PV PhysicianADIENNE 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

Manni Kuthiala, PV Affiliate – Strategic Alliance ManagerRoche 

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:


Mikhail Kryukov

Tel: +44 (0) 20 3141 0649

Email: mkryukov@acieu.net

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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Peer reviewed publication,  by its distinguished editorial advisory board, JCS provides you with the best practice guidelines for conducting global clinical trials. JCS is the specialist journal providing you with relevant articles which will help you to navigate the complex world of global clinical trials. www.jforcs.com

PharmaCircle is a leading provider of global information and analytics on drugs, biologics and combination products in all stages of development, delivering seamless integration of scientific, clinical, safety, regulatory, manufacturing and commercial information into one solution.  PharmaCircle connects product and pipeline information for drugs and biologics with formulation and component details, and provides expert analysis on drug delivery technologies and devices.  PharmaCircle’s multi-parameter search capabilities and layered analytics support the information needs of drug discovery, toxicology, pre-formulation, formulation design and development, process development and scale-up, and technology transfer.   Visit our website to see how we can help your company.


Technology Networks is an internationally recognised publisher that provides access to the latest scientific news, products, research, videos and posters. Our global community is made up of over 300,000 researchers and scientific professionals from the life science, drug discovery and analytical arenas.



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ACI has put together a range of packages to suit your requirements. These range from branding options, to full scale partner solutions and can be tailored to meet your objectives and budgets.

If you are launching a new product or service and wish to gain visibility and brand recognition within your industry, contact us today!

For commercial opportunities, please contact:

Joshua Hill

Tel: +44 20 3141 0610

Email: jhill@acieu.net

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The European Drug Safety Summit 2018 - Documentation Package Only£470.00

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The European Drug Safety Summit 2018 - Conference Pass (inc. documentation pack)£1,595.00

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