But, for various reasons — including the potential for change to jeopardize approvals — drug sponsors have been slow to adopt these innovative research methods, and the lag is costing the pharmaceutical industry huge amounts of both time and money.
TORONTO (PRWEB)
September 13, 2019
Over the last decade, the drug development industry has realized the benefits of monitoring trial conduct, safety, data integrity, compliance and enrollment through improving risk-based monitoring (RBM) methods. As a result, we are seeing several recommended changes in our approach to research.
But, for various reasons — including the potential for change to jeopardize approvals — drug sponsors have been slow to adopt these innovative research methods, and the lag is costing the pharmaceutical industry huge amounts of both time and money.
Join Jonathan Andrus, Chief Business Officer at Clinical Ink in a live webinar on Wednesday, September 25, 2019 at 10am EDT (3pm BST/UK) to hear about adopting a comprehensive RBM strategy supported by today’s newest data integration and management technologies.
His discussion will also include:
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The advantages of using eSource systems, including ePRO and eCOA, for capturing data directly from the patient - The impact of time and cost savings associated with direct data capture (DDC) including reducing site monitoring visit frequency and eliminating source document verification and review
- The power of on-demand data and a complete audit trail in study planning, decision-making and regulatory submission
For more information or to register for this free event, visit Rerouting Your Risk-Based Monitoring Strategy: Overcoming Implementation Roadblocks with New Technologies and Approaches.
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