29/06/2024 Other Services
Understanding and complying with country registration requirements is essential for successful market entry and ensuring the safety and efficacy of medical devices. Each country may have specific requirements, so it’s essential to consult the respective regulatory authority’s guidelines and possibly seek assistance from regulatory consultants specializing in medical device registration.
We at Maven constantly stay updated with the dynamically changing regulations and requirements and keep our clients who have used our services updated with any changes in respective regulations and also send across reminders when their registration are due expiry.
CountryRegistration
MedicalDevice
IVDDevice
CountryRegistrationRequirements
Understanding and complying with country registration requirements is essential for successful market entry and ensuring the safety and efficacy of me...
Premarket Notification 510(k) is not required before marketing Class I as well as some Class II dental medical devices in the United States. ITB HOLDI...
CDSCO Registration is mandatory to approve and regulate pharmaceuticals and medical devices in India, overseen by the Central Drugs Standard Control O...
Sunglasses, spectacle frames, spectacle lens, and magnifying spectacles are medical devices exempt from the Premarket Notification 510(k) submission t...
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