Government Registration
Medical Devices Registration
Service Overview
CDSCO registration for import, manufacturing, or sale of medical devices under Medical Devices Rules.
Documents Required
Please keep the following documents ready for smooth and prompt processing of your application:
- ISO 13485 Certificate
- Device Specifications
- Master File
- Quality Management System details
Our Execution Process
1
Submit Enquiry / Documents
Fill out the consultation form on the right. Our expert will call you to clarify requirements and verify your documents.
2
Application Drafting & Filing
We prepare the requisite legal documentation, board resolutions, or government challans and submit them to the respective authority.
3
Tracking & Delivery
We track your application status in real-time, handle any departmental queries, and deliver the final registration certificate/receipt.