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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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CBSD
Center for Biomedical System Design

Our mission is to improve health outcomes by accelerating appropriate, timely, and equitable patient access to biomedical products in ways that work for all stakeholders.

Tufts Medical Center
800 Washington Street, Box 63
Boston, MA 02111

tuftsmcnewdigs@tuftsmedicine.org

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