- Medical Device Registration 2025

How To Apply for Loan License?

Let me explain the process apply for loan license. It is straightforward. A loan license allows you to manufacture products using someone

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

Innovative Devices for Clinical Trial Form MD-28 New IVD

The Innovative Devices for Clinical Trial Form MD-28 is an important document for devices that are discovered and newly introduced to the

What Does Schedule Fourth of MDR 2017 Include?

This article, Schedule Fourth of MDR 2017, provides a list of comprehensive documents required for Schedule Fourth Medical Devices Rules (MDR) 2017.

What Is Premarket Approval?

The FDA, also known as the Food and Drug Administration, uses Premarket Approval to ensure that class III MDRs are effective or

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

What Is A Drug License?

This question is widely asked: what is a Drug License, and is it the most straightforward term to know what it means?

What Is The Ethics Committee For Clinical Trial

Many people are unfamiliar with the Ethics Committee for Clinical Trials. The Ethics Committee reviews and ensures that human medical device research

What Is The Difference Between Bioavailability And Bioequivalence Studies?

If you want to know the difference between bioavailability and bioequivalence studies, then your answer is here, and it’s designed for you

What Are The Legal Requirements For Drug Labeling?

Drug labeling is governed by Rule 96 of the Drugs and Cosmetics Act and must meet specific requirements outlined by the Central