The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act, 1965, (Act No. 101 of 1965) as amended, to provide for the monitoring, evaluation, regulation, investigation, inspection, registration and control of medicines, scheduled substances,...
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Review and verify all licence applications, Check all licence applications for completeness, correctness, and compliance, Reconcile and prepare reports, Imports and exports reconciliations, Follow up on defaulters, Follow up on non-renewals and non-returns, Process and update information on the database relating to: (Inspections and communicate non-compliances to Radiation Scientists, Source exchanges, Imports and exports), Process information related to radiation over-exposure on the database....
Qualification :
Matric certificate and a BSc (Physics or Medical Physics) or a B. Rad. (Diagnostic/Nuclear Medicine/Radiotherapy) qualification.
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