Medical Device Registration
Medical device registration is a crucial regulatory process that ensures the safety, efficacy, and compliance of medical products before they enter the market. It involves approvals from authorities such as the FDA, CDSCO, CE marking, or ISO certifications, depending on the region. Proper registration helps prevent legal issues, protects patients, and facilitates global trade.
Our Services
Manufacturing & Import License
Ensures compliance with medical device regulations for manufacturing and importing products under relevant rules and forms.
Medical Regulatory Compliance
Supports adherence to national and international medical regulations, ensuring products meet safety and quality standards.
CDSCO Registration
Facilitates registration with the Central Drugs Standard Control Organization, ensuring devices meet Indian regulatory requirements.
Export Compliance
Helps meet export regulations, including AEO Certification, US FDA, and EU CE ]Marking for global market entry.
Green Compliance
Ensures environmentally responsible waste disposal and obtains necessary NOCs from pollution control boards.
AccorpMed streamlines medical compliance with expert licensing and certification solutions. Trusted by 100+ healthcare businesses, we ensure hassle-free approvals for land, product, labor, and distribution licenses.
Contact Information
support@accorpmed.com
+91 99682 97717
909, ITL Twin Tower, B-9, Netaji Subhash Place, Pitampura, Delhi-110034 (INDIA)
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