Classification of Medical Devices by CDSCO in India
by Yash Chauhan on 2023-04-28
To solve this problem, the Medical Device Division of Central Drugs Standard Control Organization of India (CDSCO) issued a notice in 2020 and provided a classification of the medical devices into different categories and four classes which are A, B, C, and D.
Procedure for Manufacturing of Class C and Class D Medical Devices in India
by Shamshad Alam on 2023-04-27
The CDSCO can reject the application for the grant of Class C and D medical devices manufacturing licences on the ground of valid reasons.
ISO 14064 - Greenhouse Gas Emission Validation and Verification
by Yash Chauhan on 2023-04-26
It was developed by 175 experts from 45 countries and took four years to fully get developed. In this article, we will discuss everything about the standards laid down in ISO 14064, their applicability, compliance and benefits.
Green Standards to Address issues of Sustainability by BIS
by Yash Chauhan on 2023-04-21
It is involved in the formation of green standards as per the National Action Plan for Climate Change provided by the Government of India.
Export of Medical Drugs from India to USA
by Shamshad Alam on 2023-04-13
If you are one of them, read this article till last because, in this article, we will discuss existing rules and regulations prescribed by the Government of India for the export of Medical Drugs from India to the USA (United States of America).
New Drug Approval Rules by CDSCO
by Yash Chauhan on 2023-04-12
CDSCO is responsible for approving drugs, conducting clinical trials, setting standards for drugs, ensuring the quality of imported drugs, and coordinating with State Drug Control Organizations to enforce the Drugs and Cosmetics Act.