Table 1.

The Main Content Items of hESCreg Are Shown, Comprising Ethics and Regulatory Documentation, Scientific Characterization, Provider Information, and Additional Information

Ethics and regulation	Cell characterization	Provider/user
Origin of the cell	Donor phenotype	Identification of cell line generator, owner, and distributor
Informed consent documentation	Derivation process	Institution/country
Evidence for regulatory compliance	Genotype	Specific restrictions on cell availability
Data protection measures	Expression/marker profile
	Evidence of functional pluripotency	Communication tools/feedback
Specific restrictions	Subclones/control lines/genetic modifications
Additional information (protocols, quality control data, applications, research projects)

The minimal registration criteria are shown in bold.