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Quality System Regulation (QSR) – Process and Importance

In the highly regulated industry of medical devices and pharmaceuticals, ensuring quality, safety and compliance is of the utmost importance. The Quality

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Medical Device Import License

What Is Medical Device Import License?

If are you a part of the medical device industry then you must be aware of its regulatory compliance process as per

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How To Apply Import License For InVitro Diagnostics Medical Devices?

When you have to import any of the IVD devices in India then you must apply import License for InVitro Diagnostics Medical

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Difference Between DCGI And CDSCO

The difference between DCGI and CDSCO is very confusing and hard to understand so here is the easy differentiation between CDSCO &

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CDSCO Registration for Tongue Depressors

CDSCO is the Indian Regulatory Authority that is responsible for ensuring the safety, efficacy & quality of medical devices & pharmaceuticals. The

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In-Vitro Diagnostics Medical Devices

If you are willing to understand In-Vitro Diagnostics Medical Devices before dealing with them, then you are in the right place. Here

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Medical Device Loan License Post Approval Changes

In the medical device manufacturing world, it is very common for manufacturers to operate under a loan licence. A loan licence is

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ISO 14001:2015 Environmental Management Systems

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Let’s understand the ISO 14001:2015 environmental management system because organizations are continuously becoming aware of the effect on the environment. Whether it’s

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List of 2014 Approved Drugs In India

The drug ontroller genral of india (DCGI) provide 2014 approved drugs in india list with a wide range of pharmaceutical drugs. It

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List of 2018 Approved Drugs In India

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The approval of new drugs in the market plays a very crucial role in advanced healthcare. It ensures the availability of safe

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