Middle East Markets

Complete SFDA regulatory compliance solutions for medical devices and healthcare products.

• SFDA Medical Device Marketing Authorization
• Product Registration and Listing
• Quality System Requirements
• Post-market Surveillance

Comprehensive MOHAP regulatory pathways for medical device market authorization.

• MOHAP Registration
• Technical Documentation Preparation
• Emirates Standard Conformity
• Market Authorization Services

End-to-end TITCK regulatory services for Turkish market entry and compliance.

• TITCK Product Registration
• Medical Device Technical Documentation
• Local Authorized Representative
• Vigilance and Market Surveillance

Complete regulatory services for medical device registration in Israel.

• AMAR Registration
• Medical Device Import License
• Quality System Certification
• Clinical Trial Applications

Regulatory pathway for medical devices entering the Iraqi market.

• Kimadia Registration
• Import License Applications
• Product Listing Services
• Market Access Support

Complete medical device registration services for Qatari market.

• MOPH Registration
• Product Conformity Assessment
• Import Permit Applications
• Market Compliance Monitoring

Regulatory compliance services for medical devices in Kuwait.

• MOH Registration
• Product Approval Process
• Import Authorization
• Quality Assurance Requirements

Regulatory services for medical device market entry in Iran.

• Iran FDA Registration
• Import License Applications
• Customs Clearance Support
• Market Compliance Services