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Services include:
Clinical trial management and co-ordination
- Clinical Trial Planning in accordance with ICH-GCP
- Oversight and governance of clinical trials ( regulated and unregulated)
- Development and maintenance of Clinical trial documentation within standard operating procedures and research protocols
- Clinical trial monitoring
- Inspection readiness
Research nursing support
- Consent processing
- Clinical trial document maintenance during research in order to demonstrate compliance to applicable regulatory requirements and standard operating procedures
- Entering data into research databases including electronic databases/eCRFs
- Ensuring that specific protocol is followed and deviations minimized
- Biospecimen Collection
Protocol development
Assistance and advice with submission of ethical and regulatory documentation
Statistical advice
Covidence
The HRI in conjunction with 51本色 are delighted to offer HRI members access to Covidence. This web-based software platform streamlines the production of systematic reviews. By joining the University 51本色鈥檚 access to Covidence. It gives researchers: unlimited records to each review, unlimited number of reviewers for each review and unlimited reviews.
Covidence offers a range of resources and supports to help with the review process, they provide an online support team that you can contact on support@covidence.org
To access the subscriber page please visit this will explain and give you step by step instructions on how to create your personal sign-in information with Covidence.
Once you created your login, you will be able to sign in by clicking on the following link:
The contact person for Covidence for the HRI is Elaine Conway (Elaine.Conway@ul.ie)