Join the Consent 4 Consent database to help with research

Mae’r cynnwys hwn wedi dod o wefan allanol ac mae ar gael yn Saesneg yn unig.

Research is the only way to improve our understanding of illness and to build evidence to develop better treatments in the future. Nearly all research needs the help of volunteers in order to develop these procedures and find out whether they are effective.

The North Wales Clinical Research Facility (NWCRF) has developed a secure database of volunteers who are willing to be contacted about future research projects called Consent 4 Consent (C4C). C4C is an internal database for safely taking, storing and utilising a written record of consent for patients and healthy volunteers who wish to be considered as potential participants for research projects. 

If you agree to be included on the C4C database then research professionals from the NWCRF will be able to contact you if there is a research study that they think may be of interest to you. The researchers will then send you information about the study and also give you the chance to ask any questions.

Join the C4C database by emailing the NWCRF research team.