Navigating CDSCO registration can be complex, but I’m here to make the process seamless for you. Whether you need assistance with import, manufacturing, or sales licenses, I provide expert guidance on documentation, compliance, and regulatory approvals under India’s Medical Device Rules (MDR), 2017. From preparing technical dossiers to ensuring compliance with labeling and Unique Device Identification (UDI) requirements, I handle all aspects of registration. My expertise covers all medical device classes (A, B, C & D), ensuring a hassle-free approval process with the Central Drugs Standard Control Organization (CDSCO). Let’s work together to get your medical devices registered efficiently, avoiding delays and ensuring full regulatory compliance.