- Medical Device Registration 2025

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

What is ISO/IEC 27001?

ISO/IEC 27001 is the international standard for managing information security. It provides a systematic approach to protecting sensitive company data, whether it’s

Manufacturing Registration Post Approval Changes For Medical Devices

Once your medical device is authorized, it might feel like the finish line, but don’t celebrate just yet, there’s more to consider.

Mandatory CDSCO Registration for Class A Devices in India

To all those who are willing to enter the industry of medical devices as a manufacturer, distributor or importer, CDSCO registration is

GMP Audit In Pharma [Meaning, Process & Guidelines]

In the intensely regulated pharmaceutical world, a GMP audit guarantees conformity with Good Manufacturing Practice, ensuring product quality and patient safety. These

What Are Form MD 7 and MD 9?

Form MD 7 and MD 9 are essential for obtaining in the medical device manufacturing industry. If you are a manufacturer of

MD 41 & 42 License [Wholesale License For Medical Devices]

With growing demand for healthcare products, the indian government has made strict regulations in place to provide safety & quality of medical

CDSCO Registration for Stethoscope

In India, the medical instrument industry is mainly handled by the regulatory Central Drugs Standards Control Organisation (CDSCO), assuring that items such

What Is CDSCO?[Process, Documents & Importance]

In the modern world of healthcare and consumer products, compliance with CDSCO regulatory standards isn’t just good practice, but essential. If you

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.