Medicines and Related Substances Control Act, 1965 (Act No. 101 of 1965)

13. Registers

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(1)The Chief Executive Officer shall keep separate registers for medicines, medical devices or IVDs, in which he or she shall record—
(a)the registration of medicines, medical devices or IVDs by the Authority; and
(b)such particulars in regard to the medicines, medical devices or IVDs and the holder of certificate of registration in respect of such medicines, medical devices or IVDs as are required by this Act.

 

(2)The Chief Executive Officer shall publish on the Authority’s website the registers referred to in subsection (1) and update those registers when registration is obtained.

 

[Section 13 substituted by section 6 of Notice No. 19, GG 39585, dated 8 January 2016]