The previous email included the wrong webinar information. Please see the corrected information below: For biopharmaceutical developers, designing a time- and cost-effective clinical strategy from product inception to regulatory approval is essential for meeting early-phase clinical trial objectives.Therefore, an in-depth understanding of adaptive clinical trial design and logistics is critical. In this interactive webinar, Dr. Jignesh M. Patel of Cardinal Health Regulatory Sciences will provide the framework for scientifically robust and efficient early-phase clinical drug development. Working with cross-functional teams and developing appropriate operational infrastructure for all stakeholders, including drug developers, clinical research organizations (CROs) and investigator sites, will also be highlighted. Register Now
| Date: Thursday, August 3, 2017 Time: 2pm ET / 11am PT Duration: 1 hour |
About the Speaker: | Jignesh Patel Principal Scientist Cardinal Health Regulatory Sciences |
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