Trusted MDR Consulting | MD5 Manufacturing Licenses | MD9 Import Licenses – GQA Consultants

End-to-End Regulatory Support for Medical Devices in India CDSCO Registration • MDR Compliance • MD5 Manufacturing License • MD9 Import License Trusted Consulting for Medical Device Manufacturers & Importers. GQA Consultants Pvt. Ltd. provides end-to-end regulatory support for medical device manufacturers and importers as per the Medical Device Rules (MDR), 2017. Our expert regulatory team assists clients in obtaining: MD5 Manufacturing License for Class A & B medical devices MD9 Import License for overseas manufacturers CDSCO registration and regulatory approvals Technical documentation, plant layouts, QMS implementation, risk management and regulatory audits With a decade of experience, GQA Consultants ensures 100% compliance with CDSCO MDR requirements, faster approvals, and smooth documentation support for both domestic manufacturing and global imports.