For medical device regulations in India, do I follow CDSCO or BIS ?



Regulation for Medical Devices in India is by standards required by BIS or as mentioned by CDSCO (Central Drugs Standard Central Organization)

In CDSCO list few products are required to be notify but in BIS (Bureau of Indian Standards) many standards requirements are mentioned. Which we have to follow?

There is any relation between them?

Is there any requirement to place Medical devices in India market?
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Re: For medical device resulations in India, do I follow CDSCO or BIS ?

A Quick Bump!

Can someone help?

Thank you very much!!
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