Comprehensive planning early in your research will pay dividends. Use the links provided here for advice in designing your study and how to obtain correct regulatory approval. Visit the SOP and Templates page for instructions and a range of guidance documents including protocol, participant information sheet and informed consent form templates.
Instructions and advice for the active phase of your research, once all approvals are in place, can be found on the Study Management page.
Useful Documents and Links
- UK policy framework for health and social care research
- National Research Ethics Service/Health Research Authority
- UK Medicines for Human Use (Clinical Trials) Regulations 2004 (SI 2004 No. 1031)
- MHRA website