Author: ELT Team

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?

This term, the Legal Requirements for Drug Labeling, is introduced under Rule 96 of the Drug and Cosmetic Act. So drug labeling

What Is GMP Audit In Pharma?

So, Good Manufacturing Practices, which is also known as a “GMP” system, help guarantee that the product is safe and consistently produced

How To Apply For Drug Approval In India?

If you are dealing with pharmaceutical companies and individuals who wish to manufacture, distribute, or market drugs in the country drug approval

How To Apply For Drug License?

Are you a manufacturer, retailer or wholesaler of medicine then let us just introduce you to the drug license. It is mandatory

What Are the Different Types of Cleanroom Classes and Standards?

Cleanroom Classes are customized environments and carefully designed to sustain exceptionally low levels of dust, airborne organisms, or vaporized particles. It is

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 &

What are Class D Medical Devices?

Class-D Medical Devices are intrusive surgical products and these products are meant to be used for a short period. These Class D

What are Class C Medical Devices?

If you are confused about what are Class C medical devices then here is your answer, Class C medical devices are moderate

What are Class B Medical Devices?

Class – B are minimally invasive medical devices, you can also call them low-risk devices for example – Heat therapy gel, Foot