| • Updated database for regulatory requirements |
| • Local and central (GCC) registrations |
| • Preparation & submission of company and product registration dossier
|
| • Follow-up of on-going registration procedures
|
| • Supervision on existing license portfolio.
|
| • Close surveillance over regulatory developments in the region’s healthcare industry.
|
| • Scrutiny and approval of all commercial claims
|
| • Designing of protocols for post-sales clinical studies |
