Patients and patient organisations need to be involved in the process of research and development from the beginning and not as an afterthought.
Patient Public Involvement
From setting research priorities – Research design and planning – Research conduct and operations Dissemination communication post approval. Patients are often neglected in their capacity to participate in research and development as a whole.
In view of this we have set up a social enterprise that will offer the following services:
- Expert Patients/Parents
- Patient Advocacy
- Reviewer, Protocol design & literature, Study logistics, Informed consent, Patient Information, Informed consent, Protocols and Health Technology Assessment (HTA), Evaluating & Reviewing PROMs.
- Patient Recruitment, Research participant and retention.
- HTA – Patient friendly HTA report summaries, Dissemination.
Contact us today to discuss how we can support your research.