Some moments mark the start of a breakthrough and for Minerva Research Solutions, this is one of them. We are making our first-ever appearance at the Global Site Solutions Summit (SCRS) 2025, happening September 28th to October 1st in Orlando, Florida, and we couldn’t be more excited to present the solutions we have designed specifically to fit the needs of clinical research sites and sponsors. Booth# 1001 awaits your presence to discuss your challenges and deliver personalized solutions for your sites.

Why the Global Site Solutions Summit Matters?

For insights into the future of clinical research, there’s no stage more fitting than one designed to define it. The Global Site Solutions Summit is where the clinical research industry gathers to solve challenges, share breakthroughs, and shape the future of trials. This year promises:

  • 1,700 attendees bringing diverse perspectives
  • 200+ expert speakers delivering game-changing insights
  • 900 organizations united in driving research forward

For Minerva, this debut is more than attendance, it’s a chance to present how our complete trial back support helps research sites and sponsors achieve precision, efficiency, and compliance, all under one roof.

Our Core Solutions for Clinical Trials

We’re bringing four specialized services designed to maximize trial performance:

  • Patient Recruitment – Connecting you with the right participants, faster.
  • Data Operations – Managing and processing data with speed, accuracy, and compliance.
  • Regulatory Compliance – Ensuring every step aligns with FDA and GCP standards.
  • Study Launch Support – Getting trials started on time, stress-free.

Find Us at Booth #1001

Our representatives will be on hand to share expertise, discuss site needs, and explore innovative solutions:

Danial Hassan

Sr. Medical Affairs Manager, Minerva Research Solutions

Bilal Mir

Business Development Manager, Minerva Research Solutions

About Minerva Research Solutions

Minerva Research Solutions is a clinical trial management service provider dedicated to delivering high-quality data and operational excellence. With streamlined processes and specialized departments, we manage every aspect of trial operations. Our skilled team, equipped with strong clinical backgrounds, ensures adherence to FDA and GCP regulations in all trial phases. We partner with research sites and sponsors to execute trials efficiently, cost-effectively, and with complete compliance.

Address:

28260 Franklin Rd,
Southfield, MI 48034