CDSCO Registration For Software as Medical Device (SaMD)
If you want to develop or import software for medical purposes, you must get a CDSCO Registration for software as medical device(SaMD).
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If you want to develop or import software for medical purposes, you must get a CDSCO Registration for software as medical device(SaMD).
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To ensure safety and effectiveness Medical devices used in general hospitals for orthopaedics must have a CDSCO license to manufacture hospital and
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Are you the one who is willing to manufacture IVD medical devices in India then you must undergo the procedure to obtain
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The Central Drugs Standard Control Organization (CDSCO) oversees the registration of IVD in India. The number of IVD devices requiring complete technical
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In India, Medical Devices are regulated by the Central Drugs Standard Control Organization (CDSCO). Only the Notified Medical Devices have been regulated
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Those dealing with medical devices must understand the importance of medical device compliance in India. This will ensure the medical device’s safety
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CDSCO has issued essential guidance on retention of import license in India. This process is coming into effect under the new rules,
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This is your go-to guide if you want to understand Extended Producer Responsibility (EPR) in detail. EPR Annual Compliance refers to the
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The Quality System Regulation, in short, QSR, is a set of standards and rules introduced by the authorities to ensure that medical
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The Procedure to apply for InVitro Diagnostic import license is followed. Initially, evaluation of the product is to be done to ascertain
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