- Medical Device Registration 2025

Integral CDSCO License for Self-Testing IVDs in India

Navigating the landscape of medical regulation can be haunting, especially for those interested in self-testing IVD diagnostics in India. The interval of

CDSCO License for Anesthesiology Devices in India

When you are a manufacturer, importer or wholesaler of medical devices then you must understand the licensing process. It includes licenses of

What Are CDSCO Form MD-26 And MD-27?

If you are an importer and you want to Import medical devices into India, then both Form MD-26 and MD-27 are important

Difference Between FDA and CDSCO

Are you aware of what is FDA and CDSCO? If not then here we are to explain you difference between FDA and

CDSCO License For ENT Medical Devices

In India, CDSCO (Central Drugs Standards Control Organization) issues the license for the manufacturing, import, sale and distribution of medical devices. The

Definition of Medical Device As Per MDR 2017

Medical Devices are widely used in all branches of medicine, surgery and community not only in India but across the globe. To

CDSCO Medical Device Registration for Pacemaker

Are you an importer or manufacturer of pacemaker medical devices? Then here comes the necessary guide for you. To regulate pacemakers within

MD 5 License For Manufacturing Of Class A and B Medical Devices

If you manufacture medical devices in India, you must obtain a manufacturing license from the regulatory authority of India. Manufacturing license for

How To Download CDSCO Certificate?

The CDSCO ( Central Drug Standard Control Organization) plays a vital role in ensuring that products like cosmetics, pharmaceuticals, and medical devices meet

How to Check CDSCO Approved Drugs?

The Central Drug Standard Control Organization is the Indian Regulatory Body that governs all the rules and regulations for the approval of

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.