Managing your specialised register
There are a variety of training resources available to help you manage your specialised register with CRS Web.
Videos and quick reference guides
A range of short training CRS Web videos and PDF Quick Reference Guides have been produced by the CIS support team.
Webinar and training recordings
CIS Handbook (Chapter 4) - useful information on developing and maintaining your specialised register.
Best practice guidance for reporting on specialised register maintenance - a document giving guidance on where and how maintenance of a Cochrane specialised register should be reported. The guidance was produced by CIS Support and approved by the CIS Executive.
CRS import filters
CRS search syntax
A guide to CRS search syntax.
Randomised controlled trials, quasi-randomised controlled trials, controlled before and after studies and interrupted time series are the study designs eligible for publication in CENTRAL. The CERT group have produced guidance on which other reports may be eligible for publication:
The HarmoniSR Guidance for formatting core (or mandatory) fields in reference and study records in the Cochrane Register of Studies (CRS)
- Final report
- CRS core field guide: references
- CRS core field guide: study records
- CRS core field guide: books and theses
- HarmoniSR Webinar: A special webinar on applying the HarmoniSR rules in CRS Web, and how authority records might work in the future.
Identifying RCTs - Crowd tasks for identifying RCTs
Identifying trials - resources for searching for and identifying trials.
CRGs will not be granted full exemptions from maintaining specialized registers. However, modification to the traditional model of maintaining a Specialised Register may allow alternative contribution to the collective effort of identifying RCTs where an exemption is requested. For more information see the Editorial and Publishing Policy Resource Policy & procedure for managing requests from Cochrane Groups for exemption from maintaining a Specialised Register