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Past event: European Clinical Quality Risk Management Forum

Effective Risk-Based Approaches for Optimizing Clinical Quality and Achieving Inspection Readiness

The European Clinical Quality Risk Management Forum in London on 24 - 25 February, provides a forum for senior-level clinical quality, compliance and operations executives from leading pharma, biotech and medical device companies, to candidly discuss strategies for ensuring trial integrity through proactive clinical risk management.  Learn from this experienced group and take-away proven, results-driven, risk-based strategies for optimizing your company's clinical quality to achieve a continual state of inspection readiness.


This event is designed for professionals from pharmaceutical, biotechnology and medical device companies; CROs; and other clinical service providers who have responsibilities in the following areas:
  • Quality Management/Clinical Quality Management     
  • Clinical Quality Assurance/QA/CQA
  • Clinical Quality Control/QC/CQC
  • Clinical Operations/Management/ Research/Development
  • Compliance/Clinical Compliance/Regulatory Compliance
  • Monitoring/Site Management/Study Management
  • Clinical Outsourcing/Vendor Management/ Third-Party Management
  • Good Clinical Practice/GCP
  • Auditing
  • Clinical Risk/Risk Assessment
  • Regulatory Affairs
  • Medical Affairs

The event is also of interest to:
  • Investigative Sites
  • Academic Research Sites
  • Central, Imaging and ECG Labs
  • IVRS Companies
  • EDC Companies
  • Other Clinical Service Providers


  • Brigid Flanagan, The Avoca Group, Senior Consultant
  • David Fryrear, ASTELLAS, Senior Vice President, Head of Clinical and Research Quality Assurance
  • Karen Hue, AIMMUNE THERAPEUTICS, Quality Assurance Director, Europe
  • Kerstin Koenig, MERCK, Vice President, Global Head Research and Development Quality
  • Katharina Kurpanek, THE QM COMPANY; Former BfArM GCP INSPECTOR, Managing Director
  • Olga Martinez-Cesares, GLAXOSMITHKLINE, Global Quality and Training Manager
  • Rebecca Merlina, ENDOCYTE, Vice President, Quality
  • Heike Reinstaedtler, GSK VACCINES, Head, Clinical and Medical Quality
  • Devry Spreitzer, ASTELLAS, Director, Global Electronic Systems Quality Assurance
  • Paula Walker, MA, BSc, MHRA, Inspectorate Unit Manager, GCP/GPvP/GLP
  • Rebecca Webb, ABBVIE, Director, Pharmacovigilance Quality Assurance

Please fill in your name and email to receive the Conference Agenda of this event.


London Marriott Hotel Regents Park
128 King Henry's Rd, NW3 3ST
London, UK

Room Rate: GBP162.50 Single incl. VAT/ GBP215.50 Double Inc. of VAT

Reservation cut off Date: January 13, 2020 

Click here to make the reservation.

During working hours from 9-5:30 GMT please call +44 207 449 4418, or outside of working hours +44 800 221 222  and use the reference code: POJ
Event details
Organizer : ExL
Event type : Conference
Reference : ASDE-21776