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🔧 Clinical Research Support Services

Our services are designed to support the full lifecycle of clinical trials and health research projects, ensuring compliance with regulatory standards and best practices.

Clinical Trial Management and Support

• Clinical trial planning in accordance with ICH-GCP guidelines
• Oversight and governance of regulated and unregulated clinical trials
• Development and maintenance of clinical trial documentation aligned with standard operating procedures and research protocols
• Clinical trial monitoring and inspection readiness
• Research nursing support, including consent processing and biospecimen collection
• Maintenance of clinical trial documents during research to demonstrate compliance with regulatory requirements and SOPs
• Data entry into research databases, including electronic case report forms (eCRFs)
• Ensuring adherence to study protocols and minimising deviations
• Protocol development and statistical advice
• Assistance with the submission of ethical and regulatory documentation

Systematic Review Support with Covidence

The HRI, in collaboration with the ¾ÅÉ«ÊÓƵ, provides HRI members with access to Covidence—a web-based platform that streamlines the production of systematic reviews.

Through UL’s institutional access, researchers benefit from:

• Unlimited records per review
• Unlimited reviewers per review
• Unlimited number of reviews

Covidence also offers a range of resources and an online support team, available at support@covidence.org.

To get started, visit the ¾ÅÉ«ÊÓƵ & Covidence subscriber page for step-by-step instructions on creating your personal login. Once registered, you can sign in at:

For further assistance, contact Elaine Conway at Elaine.Conway@ul.ie.