Singapore legislation
Regulation 38
of Health Products (Cell, Tissue and Gene Therapy Products) Regulations 2021
Regulation 38
Duty of supplier of unregistered Class 1 CTGT product to provide information
Where a CTGT product would have been assigned to Class 1 had it been registered and the CTGT product is supplied without being registered in accordance with regulation 18, the Authority may, under section 41(1) of the Act, by notice, require the supplier of the CTGT product to provide to the Authority, within the time specified in the notice, the name and address of the manufacturer, importer or wholesaler (as the case may be), from whom the supplier obtained the CTGT product.