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Need Class A Medical Device Register assistance? Class A medical devices must be registered and comply with the Medical Devices Rules, 2017 before they are manufactured or marketed in India, as applicable. Agile Regulatory provides expert support with documentation, CDSCO application filing, regulatory compliance, and registration guidance. Our consultants help manufacturers and importers complete the registration process efficiently while ensuring compliance with applicable CDSCO requirements.

Need Registration in GeM Portal to sell products or services to government departments? Government e Marketplace (GeM) registration allows businesses, manufacturers, and service providers to participate in government procurement opportunities. Agile Regulatory provides complete assistance with GeM seller registration, profile creation, document preparation, and compliance support. Our experts simplify the registration process, helping businesses complete their GeM portal registration efficiently and access new government business opportunities across India.