The database contemplated in section 36(2) of the Act must contain the following information:
| (a) |
Particulars of each authentication service provider whose authentication products or services have been accredited, as follows: |
| (i) |
The name and, where applicable, registration details of the authentication service provider; |
| (ii) |
The names and a technical description of the accredited authentication products and services by type and class; |
| (iii) |
The business address, telephone number, website address, e-mail address and facsimile number of the authentication service provider; |
| (iv) |
The identification number and website location of the repository of the authentication service provider; |
| (b) |
A description of the accreditation processes and requirements, functions and services offered by the South African Accreditation Authority; |
| (c) |
The complaints procedures for subscribers to accredited authentication products and services; |
| (d) |
Suspended and self-terminated accreditations and recognitions; and |
| (e) |
The contact particulars of the South African Accreditation Authority. |
Medicines and Related Substances Act, 1965
