The National Institute for Health and Care Excellence (NICE) provide a user guide for submission of evidence as part of the single technology appraisal (STA) process. It explains what information NICE requires and the format in which it should be presented. The following has been taken directly from the NICE website:
Information should be submitted in the company evidence submission template. Companies making evidence submissions to NICE should also refer to the NICE guide to the methods of technology appraisal, particularly section 5 (the reference case). The NICE guide to the processes of technology appraisal gives further details of procedures relating to STA submissions.
The submission should be as brief and informative as possible. The main body of the submission must not exceed 250 pages, excluding the appendices and the pages covered by the template.
The submission should be sent to NICE electronically in Word or a compatible format, and not as a PDF file. The submission must be a stand–alone document. Additional appendices may only be used for supplementary explanatory information that exceeds the level of detail requested in the template, but that is considered to be relevant to the submission. Appendices are not normally presented to the Appraisal Committee.
When making an evidence submission, companies must ensure that:
- All confidential information is highlighted and underlined in the electronic version sent to NICE.
- An executable electronic copy of the economic model is included in the version sent to NICE, with full access to the programming code. The content of the evidence submission and the content of the economic model should match.
- The checklist of confidential information (provided by NICE with the invitation to submit) is completed and submitted.
See section 3 of the NICE guide to the processes of technology appraisal for information about all aspects of information handling.
To ensure that the appraisal process is as transparent as possible, NICE considers that evidence on which the Appraisal Committee’s decisions are based should be publicly available.
NICE requires the medical director of the company to sign a statement confirming that all clinical trial data necessary to address the remit and scope of the technology appraisal as issued by the Department of Health and NICE, within the company’s or any of its associated companies’ possession, custody, or control in the UK, or elsewhere in the world, have been disclosed.
NICE considers that the definition of ‘all clinical trial data’ is not limited to conventional randomised controlled trials (RCTs), but is meant to include other types of interventional or observational clinical research methodologies, such as large simple trials, cohort studies, case control studies, or registry data. This definition is consistent with that used by the European Medicines Agency in its policy on publication of clinical data on medicinal products for human use.
NICE requires companies to consent to it being provided directly by European Economic Area regulatory authorities all clinical trial data necessary to address the remit and scope of the technology appraisal as issued by the Department of Health and NICE. NICE will only ask regulatory authorities directly after having first approached the company for the information and the company is unable or unwilling to provide the information in a timely manner.
To find out more please visit the NICE website