In Hong Kong, multiple authorities are responsible for the oversight and regulation of cellular therapy products. The Department of Health serves as the principle advising authority to the government of Hong Kong for developing and executing public health laws and statuatory functions. Additionally, Hong Kong’s Drug Office has the authority to regulate pharmaceutical products including biological products from human origin. At the time of this writing, specific laws, regulations, and guidelines could not be found on the websites belonging to the Department of Health or the Hong Kong Drug Office.
(October 2014)
AABB Publishes New Biotherapies Manual
September 18, 2026
FDA Approves Gene Therapy for Pediatric Patients With Sanfilippo Syndrome Type A
September 18, 2026
NHLBI, University of the West Indies to Host Sickle Cell in Focus 2026
September 16, 2026