CIS Markets

Complete regulatory compliance solutions for medical devices with the National Drug Administration of Kazakhstan.

• NDA Product Registration
• EAC Certification Support
• Technical Documentation Review
• Local Testing Requirements

End-to-end regulatory services for market entry through the Center for Accreditation and Development of Pharmaceuticals.

• CAD Registration
• Product Classification
• Import License Applications
• Quality System Documentation

Comprehensive regulatory pathway for medical devices with the Republican Centre for Expertise and Testing.

• RCGE Registration
• EAC Certification Coordination
• Clinical Trial Support
• Post-market Surveillance

Complete medical device registration services with the Center for Drug and Medical Technology Expertise.

• CDM Registration
• Technical File Assessment
• Local Representative Setup
• Regulatory Compliance Monitoring

Regulatory compliance services for medical devices with the Ministry of Health of Kyrgyzstan.

• MOH Registration
• Import Authorization
• Product Quality Assessment
• Market Surveillance Support

Complete regulatory pathway for medical devices with the Ministry of Health of Tajikistan.

• MOH Registration
• Import Permit Applications
• Documentation Translation & Notarization
• Quality Assurance Compliance

End-to-end regulatory services for the State Agency for Pharmaceutical and Medical Device Control of Azerbaijan.

• TAHS Registration
• Product Certification
• Local Testing Coordination
• Market Authorization Support