- Medical Device Registration 2025

How to Apply for an MD-16 License (Loan License for Manufacturing)?

An MD-16 License is a special permission granted by the Central Drugs Standard Control Organization (CDSCO) under the Medical Device Rule, 2017.

CDSCO Site Registration for Foreign Manufacturing Sites

CDSCO site registration for foreign manufacturing sites is a mandatory procedure that allows international manufacturers to legally sell medical devices or drugs

CDSCO SUGAM Portal – Login, Forms, and Application Process

The CDSCO SUGAM Portal is the official online gateway provided by the Central Drugs Standard Control Organization (CDSCO) to streamline the application

CDSCO Labeling Checklist Imported Devices

CDSCO Labeling Checklist for Imported Devices

The CDSCO labeling checklist for imported devices is a mandatory regulatory requirement that guarantees that all imported medical devices entering India follow

CDSCO Registration For Wheelchairs

Do you know CDSCO registration for wheelchairs is a legal requirement in India that applies to all types of wheelchairs, even if

CDSCO Registration for Surgical Gloves

CDSCO Registration for Surgical Gloves is important, as it is used during surgeries. It helps in ensuring hygiene, reducing infection risk, and

Medical Device Importer Registration for Samples

Medical device importer registration for samples is an important compliance step in India. Even when the devices are not designed for sale,

CDSCO Registration for Infusion Pumps

If you are a manufacturer, importer, or distributor of infusion pumps, then you are required to understand that infusion pumps are significant

CDSCO Registration for Elastic bandages

In India, CDSCO is the main regulatory body that handles medical devices, pharmaceuticals, and drugs. Its role is to assure public health

CDSCO Registration for Ophthalmic lenses (Contact lenses)

It is mandatory to ensure the safety and efficacy of medical devices, which include ophthalmic lenses (contact lenses). The CDSCO is the

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.