• Updated database for regulatory requirements.Local and central (MENA) registrations.
• Preparation & submission of company and product
registration dossier.
• Follow-up of on-going registration processes.
• 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.
•Pre-registration sales for early returns.
•Possibility for centralized registration procedure &
fast track.
•Pricing Harmonization & International referencing
system.
•Government coverage for nationals and
privatization trend.