Publication | Open Access
Third <scp>WHO</scp> Global Consultation on Regulatory Requirements for Xenotransplantation Clinical Trials, Changsha, Hunan, China December 12–14, 2018
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REPORT (d) transgenic pig facilities; (e) biomaterials and encapsulation; and (f) immunosuppression and tolerance induction. The guidance document from the Second Global Consultation (Geneva, 2011) was also included in these discussions.
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