I am a highly experienced SFDA Regulatory Affairs Freelancer based in Riyadh with over 15 years of proven expertise in managing medical device registrations and regulatory compliance.
Core Services:
- Authorized Representative (AR) Services
- SFDA Account Setup & Management
- MDMA Product Registration (Medical Devices)
- PCS Product Classification Services
- FASEH Shipment Clearance Request Submissions
MDMA Registration – Simplified Overview:
Medical Device Marketing Authorization (MDMA) is a mandatory approval from SFDA required to legally market medical devices in Saudi Arabia. The process includes accurate product classification, preparation and submission of technical documentation, compliance with applicable standards, and handling all SFDA portal requirements.
With extensive experience, I ensure a smooth, efficient, and compliant MDMA process, minimizing delays and increasing approval success rates.
Why Choose My Services:
- 15+ years of hands-on SFDA regulatory experience
- Strong understanding of SFDA systems and requirements
- Reliable, fast, and professional support
- End-to-end guidance from classification to approval
If you need expert assistance for SFDA registration or regulatory support, feel free to contact me.
WhatsApp Only: +966571760663
