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November 2013

International Conference on Rare Diseases and Orphan Drugs (ICORD)

1 November 2013 @ 12:00 am - 2 November 2013 @ 12:00 am UTC+0

Controlled Early Access for Medicines to Patients with High Medical Need: What Can Adaptive Licensing Offer for Patients Suffering from Rare Diseases?(Abstract submitted by Tony Hoos/GSK).

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FasterCures 5th Annual Partnering for Cures

3 November 2013 @ 12:00 am - 5 November 2013 @ 12:00 am UTC+0

The Art and Science of Multi-stakeholder CollaborationPanelist: Gigi Hirsch.

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Alzheimer’s Disease and Dementia Initiative

6 November 2013 @ 12:00 am - 7 November 2013 @ 12:00 am UTC+0

New York Academy of Sciences.Panel: Public Private Partnerships. Panelist: Gigi Hirsch

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February 2014

21st International Molecular Medicine Tri-Conference, Leaders in Precision Medicine Symposium

13 February 2014 @ 12:00 am - 14 February 2014 @ 12:00 am UTC+0

“Adaptive Licensing as an Enabler for Precision Medicine”Panel: Hans-Georg Eichler (EMA), Kenneth Oye (MIT), Ed Pezalla (Aetna), Mark Trusheim (MIT), & Thomas Unger (Pfizer).

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March 2014

DIA Euro Meeting 2014

26 March 2014 @ 12:00 am UTC+0

“Creating an Adaptive Pathway for Medicines to Patients–Could this Be An Approach That Fulfills the Needs of All Decision-Makers? A Roundtable Discussion.”Moderator: Andrzej Rys (European Commission, Belgium); Hans-Georg Eichler (EMA); Jurgen Windeler (IQWiG, Germany); Tomas Salmonson (CHMP/EMA); Carole Longson (NICE); Chris James (Motor Neurone Disease Association, United Kingdom); Anton Hoos (GSK).

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May 2014

NORD Corporate Council Meeting

8 May 2014 @ 12:00 am UTC+0

“Overview of NEWDIGS-Adaptive Licensing”Thomas Unger (Pfizer).

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June 2014

Global Clinical Scholars Training Program @ Harvard Medical School

13 June 2014 @ 12:00 am UTC+0

“Overview of NEWDIGS & Adaptive Licensing”Gigi Hirsch (MIT).

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DIA 2014

15 June 2014 @ 12:00 am - 19 June 2014 @ 12:00 am UTC+0

(1) “Adaptive, Progressive or Risk-Based Licensing Models: What Approaches Could Be Considered by Mature and Emerging Markets?”Panel Moderator: Lawrence Liberti (CISR). Hans-Georg Eichler (EMA) – An Update on International Developments. (2) “How Can Studies that Inform Relative Effectiveness Best Be Incorporated into Global Drug Development Plans?” Panel Moderator: Chris Chinn (GSK). Mark Trusheim (MIT) – Overview of the NEWDIGS Janus Initiative.

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October 2014

Centre for Innovation in Regulatory Science (CIRS)

1 October 2014 @ 12:00 am - 2 October 2014 @ 12:00 am UTC+0

Invited case study presentation: “NEWDIGS – What they have discovered as critical elements.”Tony Hoos (Medicines 4 Patients)

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IRGC Annual Conference 2014

13 October 2014 @ 12:00 am - 14 October 2014 @ 12:00 am UTC+0

Improving Risk Regulation: From Crisis Response to Learning and Innovation. “Session 2.3 – Managing Uncertainty over the Life Cycle of Drug Development and Use: Enhancing Adaptability and Flexibility in Pharmaceutical Regulation.”Ken Oye (MIT), Tony Hoos (M4P), Hans-Georg Eichler (EMA).

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