- Medical Device Registration 2025

List Of Class A Medical Devices in India

Class A medical devices possess the least risk exposure device category. Medical devices that come under Class A are the minimum danger

Product Standards For Medical Devices

Product Standards For Medical Devices are critical to ensure the safety, quality of medical devices and effectiveness used in healthcare. Adherence to

Requirements For the Grant Of Manufacturing License Or Loan License

Requirements For Grant Of Manufacturing License or Loan License Medical Device

If you need help with the requirements for the grant of a manufacturing license or loan license, you have landed in the

Notified Body Of Medical Device Certification

This question What is the Notified body of medical device Certification, came into everyone’s mind, and here is your go-to partner for

Import Of Medical Devices For Personal Use

Are you planning on importing medical devices into India? Whether you’re wondering how to get an import license in India or looking

Licensing Authority Of Medical Devices Approval

If you are the one who is willing to start your business in India related to Medical Devices then you must understand

How To Apply For EPR Registration Certificate?

To maintain the balance between your work and environment you must apply for EPR Registration Certificate. Because Extended Producer Responsibility (EPR) Authorization

What is EPR Registration in Waste Management?

EPR Registration (Extended Producer Responsibility) is an administrative methodology that considers makers responsible for the whole lifecycle of their items, including post-shopper

Difference Between FSSAI and FCI

The Food Safety and Standards Authority of India – FSSAI is an autonomous agency regulated by the Indian government’s Ministry of Health

What is the MD 16 and 17 Form? Documents & Process

Are you the one who is willing to apply for the test import license in India then must understand the MD 16

ELT Corporate Private Limited is a legal consulting firm specializing in medical device regulations. We offer services related to Medical Device Rules 2017, including documentation preparation and guidance on scientific, legal, and technical requirements.