South Africa
Medicines and Related Substances Act compliance, made simple
ComplianceDesk gives you 9 pre-built Medicines and Related Substances Act controls, an evidence vault, audit-ready reports, and reminders before anything falls overdue — so proving Medicines and Related Substances Act compliance stops being a spreadsheet exercise.
Every Medicines and Related Substances Act control, organised for you
The real control library ComplianceDesk seeds the moment you activate Medicines and Related Substances Act — 9 controls across 3 categories.
Licensing
- MED-1.1 Licence held for each regulated activity
- MED-1.2 Responsible pharmacist or person appointed
- MED-1.3 Premises meet licence requirements
Quality, Storage & Traceability
- MED-2.1 Registered products only
- MED-2.2 Storage and distribution conditions controlled
- MED-2.3 Scheduled substances controlled
- MED-2.4 Recall and adverse event procedure
Marketing & Records
- MED-3.1 Advertising and marketing meets the rules
- MED-3.2 Records retained for the required period
Frequently asked questions
How many controls does ComplianceDesk track for Medicines and Related Substances Act?
9, organised into 3 categories, ready to assign to an owner as soon as you activate the framework.
Can I track Medicines and Related Substances Act alongside other frameworks?
Yes — most teams activate several frameworks at once. Controls that overlap across frameworks can share the same evidence, so you don't collect the same document twice.
How long does it take to set up Medicines and Related Substances Act in ComplianceDesk?
Activating Medicines and Related Substances Act instantly seeds its full control library. Most teams assign owners and get their first controls moving within a day.
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