Sitemap
- Medical Devices and Diagnostics
- Regulations
- Application Forms
- Registered Medical Devices and In-vitro Diagnostics Devices
- Registered Premises
- Fees and Charges Regulations
- Procedures for Marketing Authorization
- Inspection and Enforcement
- Guidelines
- Import and Export Control
- Control of Advertisements and Product Promotions
- Registration and Licensing of of premises
- Disposal of Unfit Devices and Diagnostics
- Recall of Devices and Diagnostics
- Technical Committee
- Harmonization of requirements in EAC, SADC, IMDRF, Africa and globally
- Notified Medical devices and InVitro diagnostics
- Section Profile