Get a Free Quote
Service Description:
Enlisting medical devices with the Drug Regulatory Authority of Pakistan (DRAP) is essential for market access. Tecnicare Consultant provides comprehensive services to ensure your medical devices meet all regulatory requirements. We handle the entire enlistment process, from documentation to submission, ensuring compliance with DRAP standards.
Why Choose Us:
Expertise: Our team has a deep understanding of DRAP regulations for medical devices.
Detail-Oriented: We ensure all documentation is thorough and accurate.
Continuous Support: We offer ongoing support to maintain compliance and address any regulatory issues.
Questions? You’re covered.
Requirements include product specifications, quality control measures, and relevant certifications.
The process can take several months, depending on the completeness of the application and regulatory review times.
Yes, we provide support for ongoing compliance, including post-market surveillance and reporting.