02/05/2026
Regulatory processes can create significant delays during site activation, sometimes eating up to 20–30% of the timeline. These back-and-forth approvals slow down the start of clinical trials and can impact overall efficiency.
By streamlining and fast-tracking site activation, Minerva Research Solutions helps trials increase their pace, ensuring smoother operations and timely progress.
Partner with Minerva Research Solutions to simplify site activation and keep your trials moving forward.