We support rapid activation through centralized regulatory coordination, accurate feasibility assessments, and proactive communication to minimize delays during startup.
Our investigators and research professionals bring experience across multiple therapeutic areas, with a strong emphasis on protocol adherence, subject safety, and data integrity.
We leverage community outreach, referring physicians, and internal screening workflows to support steady enrollment while prioritizing participant education and retention.
Our site operates under established SOPs aligned with GCP and ICH guidelines, with a strong culture of documentation, quality control, and audit readiness.
Sponsors and monitors benefit from timely responses, organized source documentation, and collaborative problem-solving throughout the life of the study.

Oncology is a core area of focus at Regis Clinical Research. Our team has hands-on experience supporting oncology and hematology studies across both solid tumors and hematologic malignancies, with an operational structure designed to meet the complexity of oncology protocols.

In addition to oncology, Regis Clinical Research supports clinical trials across multiple therapeutic areas, allowing our site to scale efficiently and adapt to a wide range of protocol designs and operational demands.
We welcome inquiries from sponsors and CROs seeking experienced clinical research sites for current or upcoming studies. Our team is available to discuss site capabilities, feasibility assessments, and potential collaboration opportunities.
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