- Medical Device Registration 2025

CDSCO Registration For Cardiovascular Devices

CDSCO registration for cardiovascular devices is essential if you want to import, manufacture, sell, and distribute medical devices. Cardiovascular medical devices consist

Procedure To Apply Test License for Manufacture of Medical Device

Are you a manufacturer of a small quantity of medical devices in India then you must apply test license for medical devices.

Apply Test License for Medical Devices Import

If you are willing to import medical devices, then you must understand the test license. It is mandatory to obtain it as

CDSCO License For Personal Protective Equipment In India

Here you can know about CDSCO License for Personal Protective Equipment in India, the Personal Protective Equipment (PPE), constituting a diverse array

Mandatory CDSCO License for Dental Products in India

Do you want to know if a CDSCO License for dental products in India or not then look at this here is

How to Obtain a CDSCO Import License? (CDSCO Import License)

If are you an importer of medical devices then you must understand the CDSCO Import license in India. The CDSCO (Central Drugs

CDSCO License for Dermatological and Plastic Surgery Product

Medical devices that are used in dermatological and plastic surgery should have a CDSCO license for dermatological and plastic surgery products to

Role of Clinical Trials in Medical Device Registration

The role of clinical trials in medical device registration is to determine whether a new device or drug is safe and effective

Role of ISO Standards in Medical Device Registration

Do you know what is the role of ISO Standards in Medical Device Registration, Any manufacturer can expect better control of the

What Is Regulatory Compliance? [Importance, Challenges & Examples]

Regulatory compliance means adhering to the laws, guidelines, regulations, and industry standards relevant to business operations. It ensures that the companies work

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.