Category: CDSCO

What Is The CDSCO Registration Process?

The Central Drugs Standard Control Organization (CDSCO) is India’s national regulatory authority for drugs and medical devices. Under the Ministry of Health and Family Welfare, CDSCO ensures the country’s safety, efficacy, and quality of medical devices. This guide outlines the CDSCO registration process, the necessary

What Is The Form 44 In CDSCO?

In simple words, form 44 in CDSCO takes permission to import or manufacture new pharmaceuticals to conduct medical trials. This article covers various required documents for Form 44 and details regarding Form 44 in CDSCO. Check out the blog. What Is The Process To Apply

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 & DCGI, their key functions, responsibilities, and more. Read to clear your confusion, know what is CDSCO & DCGI, and the role of DCGI

Common Mistakes To Avoid To Apply CDSCO Medical Device Registration

In this article, you will see the list of typical mistakes to avoid to apply CDSCO medical device registration. an Indian medical device with the Central Drugs Standard Control Organization, or CDSCO. To expedite the application process and negotiate the fairly complex regulatory landscape for

What Is CDSCO? – Process, Documents & Importance

Most medical device manufacturers want to know what is CDSCO before registration. Here comes the answer for all the curious readers to understand about CDSCO (Central Drugs Standard Control Organization) & why it is important for medical device regulation. So let’s deep dive into CDSCO

How To Apply For CDSCO License In India?

If you are a manufacturer or seller, then you should know how to apply for CDSCO license in India. Companies and individuals involved in manufacturing, selling, import & export drugs/medical devices in India must ensure that businesses follow regulatory standards for pharmaceuticals or medical devices.