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complete procedure to meet

Complete Procedure to Meet the CDSCO License Mandate of Class C & D Non-Notified Medical Devices

Overview of the CDSCO License Mandate The Central Drugs Standard Control Organisation (CDSCO) is the regulatory body that manages medical device registration in India under the Ministry of Health & Family Welfare. The main aim of CDSCO is to ensure that medical devices are...

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Infograph of the timelines for obtaining the registration for medical devices and IVD in India. The registration shall be on voluntary basis for a period of eighteen months (1st April 2020 to...

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Approval of IVD for COVID-19

World Health Organization (WHO) has declared Corona virus Disease (COVID -19) as a global pandemic. A recent coronavirus outbreak is a public health emergency of international concern due to its rapid transmission...

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New Regulations of Government of India Considers 8 Medical Devices as Drugs

Medical devices market in India is booming now. There are lots of medical device innovation and import happening from all over the world. In order to maintain quality assurance and safety, Ministry...

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Medical Devices

The Government of India is revamping the existing regulations on medical devices to be at par with the global norms and standards, to have a better control over their manufacture, import and...

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The Indian healthcare industry is one of the world’s largest healthcare setup. Being the 2nd largest population in the world, the healthcare of this burgeoning people is funded by either healthcare insurance,...

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Nowadays, therapeutic treatment based on medical devices is providing technologically advanced solutions for the management, diagnosis, treatment,mitigation or prevention of several diseases. Thus, the demand continues to grow in the market at...

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The Indian government has brought about some major changes with regards to the rules and regulations governing the manufacturing to enhance the quality of products used in the healthcare industry. As India...

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Medical Device Registration in India

The new ‘Medical Devices Rules, 2017’ have already been published and will commence w.e.f January 1st, 2018. A guidance document has been issued by the Ministry of Health & Family Welfare (MoH&FW)...

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