The Congenital Heart Research Network is a collaborative network for conducting multi-centre research in the UK and Ireland, to improve the care and outcomes of children and adults born with congenital heart disease

We are pleased to be part of the Executive Committee helping to ensure that patient priorities in research are delivered. We showcased a video at the launch event to share real stories and impact this could make.

 

 

“We are delighted that Rajwant Kaur Singh, CEO of Children’s Heart Federation, has agreed to join the Executive committee to oversee the CHD research Network. We will soon be looking for patients, parents, and family members with lived experience of congenital heart disease to join a national patient and public involvement group, to help shape this research and ensure that families remain at the center of everything that we do.” Mr Nigel Drury, Consultant in Paediatric Cardiac Surgery, Birmingham, and Director of the Congenital Heart Research Network

This is continuing our work as part of the priority setting partnership  addresses the                      priorities for research on children and adults with congenital heart disease.

 

 

 

 

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