At Cornerstone Clinical Research Services (CCRS), we specialize in helping clinical trial sites operate smoothly, stay compliant, and deliver high-quality research. Whether you're a new site looking for guidance or an established site needing expert support, we offer tailored solutions to optimize your processes and enhance efficiency.
Setting up and managing a research site can be complex, but we simplify the process with expert support in:
Get your site up and running with the right structure, systems, and processes.
Upgrading or switching Clinical Trial Management Systems (CTMS)? We streamline the transition process, ensuring a seamless integration with minimal disruption while optimizing workflows for maximum efficiency.
Assistance with IRB submissions, site regulatory documents, and ongoing compliance.
Customized source documents designed for accuracy, completeness, and audit readiness.
Well-structured SOPs are the backbone of any successful research site. We help develop, refine, and implement SOPs to ensure compliance with GCP, FDA regulations, and industry best practices.
Empower your team with targeted training designed to enhance protocol adherence, regulatory compliance, and patient safety. Our programs equip PIs and CRCs with the knowledge and confidence to lead successful trials.
Maintaining compliance and audit readiness is crucial for research sites. We offer expert support to ensure ongoing quality and regulatory adherence through:
Comprehensive pre-audit reviews to identify gaps and ensure compliance.
Ensure your site is ready for sponsor monitoring visits and inspections.
Ongoing quality assessments to proactively identify and address compliance risks.
Don't see what you're looking for? We can tailor our services to meet your site's unique needs. Contact us to discuss how we can support you!
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