Design and coordinate multi-institute studies directed at addressing the goals of the consortium.

Set up national and international patient registries and tumor banks.

Organize and establish referral networks to facilitate patient access to centers of expertise and participation in clinical research protocols.

Organize national and international symposia, workshops, and meetings on pheochromocytoma.

Establish and maintain connections with related organizations, societies, patient support groups, and funding agencies to regularly communicate new advances and activities in pheochromocytoma research.

Educate health care professionals about the latest advances in genetics, diagnosis, localization, and treatment of pheochromocytoma; Recruit and train new investigators to the field.