Meeting Global Patient Demand for Access to Medicines Prior to Approval and Launch
Produced in conjunction with the Drug Information Association (DIA)
March 20, 2012

Panelists:
Sue Barrowcliffe, Global Director of Regulatory and Medical Strategy, Idis
Richard Klein, Office of Special Health Issues, FDA

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Meeting Global Patient Demand for Access to Medicines Prior to Approval and Launch
Produced in conjunction with Pharmaceutical Executive
February 29, 2012
Now available in archive format

Panelists:
John Lagus, Vice President of New Product and Market Development, Idis
Jill Panetta, Ph.D., Chief Scientific Officer, Polycystic Kidney Disease Foundation

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