- Medical Device Registration 2025

List of 2020 Approved Drugs in India

To know all the details about the 2020 approved drugs in india, read this blog and check all the details that are

List of 2021 Approved Drugs in India

After the COVID-19 wave, many new drugs have been introduced in the market to cure all the symptoms of COVID-19. So, the

List of 2022 Approved Drugs in India

If you want to know what are the year 2022 approved drugs in india, then here is your go-to solution, as all

List of 2023 Approved Drugs in India

The list of the 2023 approved drugs in India is mentioned below. To know the name of the drugs and indication of

List of Approved Drugs in India

If you are confused and want to check the list of approved drugs in India, then here is The proper list of

What is a Clinical Evaluation Report (CER) For Medical Device?

Are you a medical device manufacturer or distributor looking to enter a foreign market? You’ve probably heard about the Clinical Evaluation Report

Medical Device Reporting (MDR)

Medical Device Reporting (MDR) plays a crucial role in ensuring the safety and effectiveness of medical devices in healthcare settings. Enforced by

What Is Investigational Device Exemption (IDE)?

Any clinical investigation, including pilot, pivotal, and first-in-human studies, needs an Investigational Device Exemption (IDE) in accordance with India’s Medical Device Rules,

What is a Risk Management File?

Ensuring the safety and efficacy of medical devices is crucial for protecting patients and meeting regulatory standards. A Risk Management File plays

Manufacturing License Risk Management ISO 14971

Manufacturing License Risk Management ISO 14971 refers to the process of ensuring safety and profitability by managing risks related to medical devices.