EFPIA MAPPs - newsletter

 

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E-NEWSLETTER
April 7th, 2015
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Interview
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Bettina_ok-newsletter 'Patients need medicines - not to die in safety': Interview with Bettina Ryll, Founder, Melanoma Patient Network Europe

Her husband's diagnosis with melanoma led biomedical scientist Bettina Ryll to change how she thinks about drug development and risk 

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Webinar
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webinar2 MAPPs - New Tools for Decision Making
April 14th, 2015 - 13:40-15:00 CET

What is the current status of MAPPs in Europe and the US?
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Featuring:

  • Luca Pani, Director General, Italian Medicines Agency
  • Gigi Hirsch, Executive Director, CBI and Program Director, NEWDIGS, MIT, USA
  • James Anderson, Head of Corporate Government Affairs, GlaxoSmithKline, UK
  • Duane Schulthess, Managing Director, Vital Transformation (moderator)
  register 2
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Survey
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survey-newsletter KUL Survey Adaptive Pathways

Please take the KU Leuvent survey on Adaptive Pathways - your opinion counts! Completing this questionnaire will only take 10 minutes of your time.

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MAPPs / Adaptive Licensing in the Media
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news Commission Expert Group on Safe and Timely Access to Medicines for Patients (“STAMP”)
European Commission
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Fast-track approvals gain traction in Europe, as EMA U.K. schemes take off
Fierce Biotech
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Regulators streamline drug approvals
Financial Times
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Behind the scenes of medicines regulation
The Pharmaceutical Journal
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Event Report: MIT’s NEWDIGS Launches New Program in Healthcare Data
MIT NEWDIGS
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Building on our own potential: A UK pathway for regenerative medicine - A report from the Regenerative Medicine Expert Group
UK Government
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Fast-tracking medicines innovation: a question of uncertainties
European Voice
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Upcoming events
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dia-logo165x115 DIA Europe 27th Annual EuroMeeting
April 13th-15th, Paris

Including a panel discussion on Adaptive Licensing. Panelists: James Anderson (GSK), Susanna Del-Signore (Sanofi), Hans-Georg Eichler (EMA), Gigi Hirsch (MIT NEWDIGS).

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4606_overview Adaptive Designs in Clinical Trials
April 20th-21st, London

This conference will review the drug development process and provide a detailed discussion of how adaptive designs are changing the development process. The main focus of the presentation will be to explore the role of adaptive sample sizing; in particular, why it is important to consider the need to reassess sample sizes during the course of a trial. It is designed for those looking to network and gain the latest knowledge from the academics, industry leaders and regulators.

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2015PhiladelphiaBanner-newsletter ISPOR 20th Annual International Meeting
May 16th-20th, Philadelphia

Including the panel “Early Access to Medicines:  What’s in it for Payers?” Panelists:  Adam Heathfield (Pfizer), Mark Trusheim (MIT); Dan Ollendorf (ICER), Adrian Towse (Office of Health Economics, London).

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EFPIA Brussels Office
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Leopold Plaza Building
Rue du Trône 108
B-1050 Brussels (Belgium)
Tel: +32 (0)2 626 25 55
E-mail: anna.szczepanska@efpia.eu
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Vital Transformation
107 Leopold III Laan
Wezembeek-Oppem, 1970
Belgium

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