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  Class A & B Devices have been regulated since April 1 and manufacturers who were registered but not Licensed on April 1 were allowed to continue manufacturing and selling while the state and central government regulators sought compliance and audit certification etc . Similar written

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Unfortunate to see PM’s ‘Make in India’ dream being bulldozed: AiMeD In an unprecedented move, India’s leading industry body – FICCI’s Medical Devices Division – joins hands with forces inimical to the Make in India drive of Prime Minister Narendra Modi, giving a body blow

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