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Online

Two-part Webinar Series: Impact of the New European Pharmacovigilance Legislation and Important Updates

Speakers

Stella  Blackburn, MD, MA, MSC, FFPM, FISPE, FRCP

Stella Blackburn, MD, MA, MSC, FFPM, FISPE, FRCP

Strategy , Consultant, United Kingdom

Dr Stella Blackburn. MB BS, MA, MSc, FRCP(Ed), FISPE, FFPM, DLSHTM, Stella studied medicine at Cambridge and Guys, working in hospital medicine before joining the pharma industry. She has worked in PhV and pharmacoepi for 35 years: in industry (11+ years) as a regulator (16+ years) and CRO (9 years). Following her MSc in Epidemiology from LSHTM, she co-developed their course in PhV and Pharmacoepi. In 1997 she joined the European Medicines Agency (EMA). Stella developed EU strategy and policy on risk management, was lead writer on the EU guidelines on this and was part of the core team implementing the 2010 PhV legislation and ENCePP. She is/was on the CIOMS IX/XI/XIII working parties and is a member of the CIOMS Executive Committee.

Joanna  Haas, MD, MSC, FACP, FISPE

Joanna Haas, MD, MSC, FACP, FISPE

Founding Partner, Haas and Partners LLC, United States

Steve  Jolley, MA

Steve Jolley, MA

Chief Executive Officer, SJ Pharma Consulting, LLC, United States

Steve Jolley is a subject matter expert in all areas of global safety compliance and signal detection, and is a frequent speaker at leading industry events. Steve has 30 years’ experience in drug safety and pharmacovigilance and has worked with over 100 clients in North America, Europe, Japan, India and China. He holds degrees in mathematics and computer science from Cambridge University, England. He is an Adjunct Professor at Rutgers University and teaches part of their Master’s degree in Drug Safety and Pharmacovigilance.

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