- Medical Device Registration 2025

CDSCO Registration for Manual Hospital Beds

In India, medical devices are handled by the Central Drugs Standard Control Organization (CDSCO), the national regulatory body that confirms the safety,

CDSCO Registration for Dental Impression Materials

In today’s growing field of dentistry, making sure that the materials utilized in patient care are of the highest quality and meet

CDSCO Registration for Infusion Pumps

If you are a manufacturer, importer, or distributor of infusion pumps, then you must understand that infusion pumps are significant in modern

Medical Device Loan License Endorsement

In the medical Industry, it is important to ensure that products are manufactured, distributed, and marketed in compliance with local regulations. This

CDSCO Registration for Thermometer (digital & mercury)

The Central Drugs Standard Control Organization (CDSCO) is the regulatory body responsible for the safety, quality, and efficacy of medical devices, including

CDSCO Registration for Endotracheal Tubes

Endotracheal tubes (ETTs) are indispensable pharmaceutical equipment that play a crucial role in managing airways in patients, mainly during surgeries, in emergencies.

How Do I Get a CDSCO Import/Export License For India?

To get a CDSCO import export licence for India, you have to understand the requirements, standards, and many other factors. However, India

Different Types of ISO Standards

In today’s world, companies that follow proper rules and regulations gain a prestigious edge. Qualitative organisations that concentrate on quality assurance, reliability,

What Is The Difference Between GCP And ISO 14155?

Do you know the difference between GCP and ISO 1455? Here is your answer: various regulations and standards are present in clinical

What is the Difference Between ISO 14971 and ISO 13485?

Do you know the difference between ISO 1497 and ISO 13485? No.Let’s understand then For manufacturers, seeking after the legitimate standards helps

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.