In the dynamic landscape of clinical research, sponsor changes can pose significant hurdles, particularly if they occur when a trial is already in progress. When a sponsor switch is prompted by a corporate acquisition, this change introduces complexities in regulatory documentation, operational continuity, and data management. The CRO faces multifaceted challenges, from renegotiating contracts and maintaining data integrity to ensuring seamless communication and preserving patient trust. Careful planning and clear communication are essential for ensuring that the trial can continue smoothly, and that regulatory compliance, patient safety, and data integrity are maintained.
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