Medical Device Portal
The Medical Device Portal, developed by CDAC for the Central Drugs Standard Control Organization (CDSCO), revolutionizes the medical device industry in India. This online platform simplifies the registration and licensing process, allowing applicants to easily submit applications, upload documents, and track their status. With its user-friendly interface, efficient processing, and transparent tracking, the Medical Device Portal has become an essential resource for the medical device sector.
Use Cases
Simplified Registration: Streamlined registration processes for greater efficiency.
Faster Processing: Reduced processing times for quicker approvals.
Enhanced Transparency and Accountability: Increased visibility and responsibility in the system.
Improved Tracking and Monitoring: Strengthened tracking and oversight of devices.
Patient Benefits: Ensures access to safe, effective devices, leading to better health outcomes and reduced risk of adverse events.
Salient Features
• Single Window Platform: Provides a unified interface for all stakeholders involved in CDSCO processes.
• Streamlined Drug Regulatory Framework: Simplifies and consolidates CDSCO processes for greater efficiency.
• Paperless Clearances: Facilitates paperless issuance of clearances by CDSCO and State Drug controllers, ensuring transparency.
• Ease of Business: Simplifies interactions for medical device manufacturers and regulatory authorities.
• Enhanced Public Access: Expands access to citizen and consumer-centric information on drug quality and standards in India.
Chief Investigator Details
Group Coordinator
E-Governance Division