GoCART work packages
Standards of care
Education and training
Policy and advocacy
Aim: Create a central EU data registry for the harmonised collection of clinical data on patients treated with gene and cellular therapies from cells and tissues of hematopoietic origin to support collaborative studies and regulatory decision making.
Aims: Develop harmonised guidelines on patient and product management for health care professionals. Reduce inspection burden and redundancies by developing and implementing consensus-driven requirements and qualification standards for clinical teams delivering gene and cellular therapies from cells and tissues of hematopoietic origin.
Aims: Develop a central portal for both patients and caregivers as well as health care professionals to access training and educational materials on cellular therapies and to streamline the training supply to minimise duplication of efforts. Develop a consensus-based curriculum that meets the needs of multiple stakeholders.
Aims: Represent and promote the interests of the GoCART coalition and its stakeholders in EU policy making by engaging with EU institutions and other relevant stakeholders.
Aims: Stimulate scientific discussion across stakeholders, facilitate the set-up of joint research projects and avoid duplication of scientific efforts.
CAR T learning resources
Clinical case discussions
GoCART hosted a webinar series for physicians in which two clinical cases were presented and discussed with a panel of CAR T-experts.