How BRP Achieved Site Activation in Under 30 Days

In clinical research, time isn’t just money—it’s impact. The faster a site is activated, the sooner patients can enroll, treatments can be tested, and life-changing therapies can move forward. At BioResearch Partner (BRP), we’re proud to consistently achieve site activation in under 30 days—a timeline that sets us apart in the industry.

Here’s how we do it.

The Challenge with Traditional Activation Timelines

In many research networks, site activation can take months due to:

Delayed regulatory submissions
Bottlenecks in feasibility assessments
Limited coordination between departments
Technology adoption gaps

For sponsors and CROs, these delays cost time, resources, and competitive edge.

BRP’s Activation Advantage

We’ve transformed the activation process from a bottleneck into a benchmark. At BRP, rapid start-up is possible thanks to:

✅ Pre-qualified, audit-ready infrastructure
All 14 of our fully integrated sites meet FDA and sponsor requirements—before a study ever begins.

✅ Dedicated start-up team
Our regulatory specialists, contract negotiators, and startup coordinators work in sync to expedite approvals, submissions, and site training.

✅ Centralized systems
With CTMS and eSource integration across all sites, we eliminate redundancy, reduce paperwork, and speed up documentation reviews.

Real-World Results

In 2024 alone, BRP initiated over 25 new trials—80% of which were activated in less than 30 days.

This includes:

Oncology Phase II trial launched in just 18 days
Vaccine study with over 300 participants enrolled within 21 days
Cardiology trial with multi-site activation in under 4 weeks

Why It Matters to Sponsors

Speed-to-activation allows sponsors to:

Stay ahead in competitive therapeutic markets
Achieve enrollment milestones faster
Reduce trial costs without sacrificing quality
Minimize delays in drug development timelines

And in an industry where each week can impact lives, that speed can make all the difference.

Tech + Talent = BRP Speed

Technology plays a critical role—but our people make it possible. From experienced regulatory leads to on-site principal investigators who prioritize readiness, we’ve built a culture of precision, urgency, and quality.

Future-Ready, Results-Driven

At BRP, we believe operational excellence should never come at the cost of compliance or care. That’s why our rapid activation model is rooted in both efficiency and integrity.

Partner with BRP and Accelerate Your Trial Timelines

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