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9.46eCTD pilot phaseV201-Mar-2013103 KB
9.50CAMs workshopsV206-Jan-2014156 KB
9.52Audit clinical PI amendmentsV103-Jan-201436 KB
9.56Correction notice: Call-up of vitamins & Minerals GG38133V110-Nov-2014315 KB
9.57Process for implementation of regulations 9 & 10V102-Dec-201499 KB
9.61Scheduling of aspirinV211-Mar-201642 KB
9.62CAMs workshop on CTDV209-Jul-201534 KB
9.63Workshop between the regulator and industry on the guideline for wholesalers wanting to perform export activities V107-Aug-201535 KB
9.64Clinical Trials workshopV111-Aug-201534 KB
9.66Rejections and Comments on RejectionV126-Jan-201642 KB
9.68Scheduling of ibogaineV111-Mar-201641 KB
9.69Rescheduling of DiclofenacV207-Oct-201644 KB
9.71Expression of Interest API Full Assessment PilotV115-Apr-201644 KB
9.73Rescheduling of epehdrine, ephedra alkaloids & phenylpropanolamineV207-Oct-201647 KB
9.74ZACTD ImplementationV103-Jun-201643 KB
9.75EOI re Pilot re Pilot for electronic submission of ADR reportsV125-Jul-201642 KB
9.76Invitation to attend Workshop on Medical Device and IVD LicensingV104-Jul-201634 KB
9.77Backlog Action PlanV117-Aug-201643 KB
9.78Position Statement: Status of Disinfectants, Antiseptics & GermicidesV130-Sep-201686 KB
9.80eCTD Go-live in South AfricaV126-Sep-201656 KB