In this free webinar, which is part of a series addressing key challenges facing clinical trial sponsors, attendees will gain insights into the importance of pre-planning for successful clinical trials. Hear about a pre-planning model that can mitigate some of the challenges in clinical trials. The model includes vendor selection and laboratory management; assay development and validation; sample tracking, shipment and processing; and data reporting and filing support.
TORONTO, April 25, 2024 /PRNewswire-PRWeb/ -- Clinical trials, whether they are the more straightforward first-in-human or the complex and multifaceted Phase III, are fraught with both foreseen and unforeseen difficulties. Moreover, the NIH and others have recognized a trend of increasing complexity in even the most straightforward of these trials.
Most Phase II and III studies have multiple endpoints, cohorts and/or treatment regimens, potentially generating millions of data points and samples from a single study. The complexity of these trials is driven by the need to ensure rigorous trial design, to address specific and expanding regulatory requirements and to address the demand for exploration of novel scientific objectives.
Without proper pre-planning and organization, increasing trial complexity can cause problems that slow or prevent successful outcomes. Working with and managing the correct vendor for your trials is critical to success and requires proper pre-planning to execute. The demand to explore novel scientific objectives comes with an increase in the need for the development and validation of assays, which can take significant time to accomplish. The large number of samples produced by these complex clinical trials comes with an increase in the complexity of sample tracking, shipment and processing. Finally, all these samples and assays generate millions of data points requiring accurate data reporting and filing support.
What steps can be taken in the pre-planning process to mitigate these challenges? Researchers must be nimble, organized and pre-plan all phases of the trial to obtain the best possible outcomes.
This webinar is part of a series addressing key challenges facing sponsors of clinical trials. In this webinar, you will learn insider tips on how best to support clinical trials with LabConnect's pre-planning model:
- Vendor selection and laboratory management
- Assay development and validation
- Sample tracking, shipment, and processing
- Data reporting and filing support
Register for this webinar today to gain insights into the importance of pre-planning for successful clinical trials.
Join experts from LabConnect, Amanda Heller, Director, FSP Solutions, Scientific Operations; Ryan Ragland, Senior Scientific Project Manager, FSP Solutions, Scientific Operations; and Sarah Henson, Program Manager, FSP Solutions, Scientific Operations, for the live webinar on Wednesday, May 15, 2024, at 10am EDT (3pm BST/UK).
For more information, or to register for this event, visit Importance of Pre-Planning for Successful Clinical Trials.
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