The voice of the patient in clinical research and development is increasingly being taken into account, from the setting of research priorities right through to dissemination of results. This marks a shift in what has historically and culturally been seen, until relatively recently, as research “on” rather than “with” patients. PPI is an inherent part…
We are working to ensure children have the same rights as adults to access high quality, evidence-based medicines and health care services. We are fully committed to increasing high quality paediatric research.
c4c will host an online ‘Train the Trainers’ workshop on 16-17 September 2020. This workshop is open to all patients and patient representatives who are interested in finding out more about the life cycle of medicines and how to get involved within the c4c project. To attend this workshop – apply here! The ‘Train the…
Check out the new c4c video – From the patient’s side – aiming to inform the public about the c4c network and how patients and their families can contribute. “At c4c we are working to give a voice to children, young people and families in research and YOU have much to say. Help us to…