Clinicians have an important part to play in supporting and promoting health care research and at Surrey and Borders we welcome and encourage our staff and students to engage in research.
Below is some useful information about the documentation needed and helpful websites that contain relevant guidance. If you have any questions about getting involved in or conducting research please get in touch with us on 01932 722 247 or email@example.com.
Is my project research?
If your study is led from England and involves the NHS in England, you should obtain Health Research Authority (HRA) approval. Before you apply for Research Ethics Committee (REC) review, please visit the applicant guidance section of the HRA website for information about how to apply.
Carrying out research at our Trust
All research activity requires Trust approval so if you are approached by external researchers about participating in a study please let us know before proceeding. You can call us on 01932 722 247 or get in touch by emailing firstname.lastname@example.org.
To gain approval for a study please complete the relevant form, based on the type of research:
UK Clinical Trials Gateway
Policies and procedures
Anyone who would like to carry out research should read and comply with our research and development policies and procedures:
- Research and development policy and procedure
- Clinical trial guidelines and procedures
- Clinical trials for investigational medicinal products policy
Researchers are responsible for submitting the correct and complete documentation to our research office in a timely manner. We suggest that prospective researchers submit in parallel to their IRAS application.
Student researchers should approach their university for help with ensuring that they understand our policies and procedures, and have all the required documentation in hand.
The following documentation is required electronically:
- Expression of Interest form. It is the researcher's responsibility to identify a Trust field supervisor to advise them who the professional lead and service manager will be. Both need to countersign the Expression of Interest
- A full or outline protocol / proposal for the study
- All attachments, addendums, appendices etc relating to the proposal
- An PDF version of the IRAS application
- An HRA approval letter and REC letter
- A MHRA approval letter, if applicable
- Confirmation from the relevant sponsor or university of insurance / indemnity cover
All external researchers who seek access to the Trust will need to obtain an honorary research contact (by submitting a research passport where appropriate), and will be issued with a letter of access before entering Trust premises.
Researchers who have a contractual relationship with an NHS body should submit the relevant documentation and request an NHS-to-NHS letter of access.
All of the documentation listed above should be emailed to email@example.com.
Legislation and guidance
- Health Research Authority Policy Framework for Health and Social Care Research in the UK
- World Medical Association Declaration of Helsinki - Ethical Principles for Medical Research Involving Human Subjects
- The Medicines for Human Use (Clinical Trials) Regulations 2004
- EU Clinical Trials Directive
- Mental Capacity Act 2005
- Data Protection Act
- Health Research Ethics Committee Governance Arrangements