Are you planning to launch a medical device in India? You’ll need CDSCO Registration to legally sell or distribute your product. Whether you’re a domestic manufacturer or an international importer, the process can feel complex, especially if you’re new to Indian regulatory requirements. That’s where Om Garuda Group steps in to simplify and accelerate your journey with expert-backed support for CDSCO Registration Online.
The Central Drugs Standard Control Organization (CDSCO) is the regulatory authority under the Ministry of Health and Family Welfare in India. It oversees the approval, regulation, and monitoring of drugs and medical devices in the country. CDSCO Registration is mandatory for all medical devices falling under notified categories before they can be sold in the Indian market.
This registration ensures that your product complies with the safety, quality, and performance standards set by the Indian government. The process may vary depending on whether the device is classified as Class A, B, C, or D, ranging from low-risk to high-risk medical devices.
Without a valid CDSCO medical device certification, your product cannot legally enter the Indian healthcare market. The certification is not just about paperwork it’s about building trust with hospitals, clinics, and consumers. It signals that your device is reliable, tested, and approved by the highest regulatory body in India.
Whether you're introducing a new surgical instrument, diagnostic equipment, or life-saving device, the CDSCO medical device certification adds credibility and legal validation to your brand.
With digital transformation sweeping across Indian governance, the CDSCO now allows applicants to complete the registration process entirely online. The CDSCO Registration Online system offers several benefits:
Faster processing time
Transparent tracking of application status
Reduced paperwork and physical visits
Convenient document uploads and communication
But while the online system offers speed, the process still requires proper classification, documentation, and technical submissions. A single error can lead to rejection or delay. That’s why many companies partner with regulatory experts like Om Garuda Group to ensure a smooth and error-free experience.
At Om Garuda Group, we specialize in guiding businesses through the end-to-end process of CDSCO Registration and CDSCO medical device certification. From product classification to document preparation and portal submission, our experienced consultants ensure that everything is aligned with current CDSCO guidelines.
Here’s how we help you fast-track your CDSCO compliance:
Free initial consultation to assess your product category
Accurate classification of your medical device (A, B, C, D)
Preparation and verification of all necessary documents
Online submission and real-time tracking
Communication with regulatory authorities, if needed
We understand the value of time in product launches and imports. Our goal is to minimize delays and get your certification completed without the usual stress or confusion.
If you fall into any of the following categories, you will need CDSCO Registration Online:
Indian manufacturers of notified medical devices
Importers of medical devices into India
Authorized Indian agents representing foreign manufacturers
Depending on your category, the documentation and approval process may vary. With Om Garuda Group, you don’t have to worry about compliance complications we handle it all for you.
The Indian medical device industry is growing rapidly, and being part of it means aligning with regulatory standards. With Om Garuda Group, you gain a trusted partner who understands the ins and outs of CDSCO Registration and CDSCO medical device certification.
We help manufacturers, importers, and agents fast-track their CDSCO Registration Online and ensure their product meets every legal and technical requirement. Don’t risk rejection or delay consult our team today and get expert support from start to finish.
Ready to simplify your CDSCO Registration process? Connect with Om Garuda Group for a free consultation. Let’s ensure your medical device is certified, compliant, and ready for the Indian market without the paperwork hassle.