Talk Small Biopharma Strategies track
What to Consider in Managing External Data for the Small Biopharma
Wed, Feb 5, 2025 · 9:15–9:35 AM EST Rosen Shingle Creek
About this session
Efficient and compliant clinical trial data management is the cornerstone of successful drug development and regulatory approval. As the volume and complexity of non-clinical data continue to grow, organizations face critical decisions about whether to manage data in-house, outsource to Contract Research Organizations (CROs), or adopt hybrid approaches. This session explores the strategic and operational considerations that influence these decisions. Attendees will gain insights into the advantages and challenges of in-house data management, the benefits and risks of outsourcing to CROs, and the flexibility offered by hybrid models, helping clinical operations professionals, data managers, and decision-makers seeking to optimize their clinical trial workflows and make informed choices that align with their organization's goals and resources.
