- Medical Device Registration 2025

List of 2014 Approved Drugs In India

The drug ontroller genral of india (DCGI) provide 2014 approved drugs in india list with a wide range of pharmaceutical drugs. It

List of 2018 Approved Drugs in India

The approval of new drugs in the market plays a very crucial role in advanced healthcare. It ensures the availability of safe

List 2015 Approved Drugs In India

Are you looking for the comprehensive list of the 2015 approved drugs in India, by the Central Drugs Standard Control Organization (CDSCO)?

ISO 17665 Sterlization of Health Care Products

ISO 17665 Sterilization of Health Care Products

Sterilization is the backbone of safe healthcare practices, ensuring that medical devices are free from harmful microorganisms like bacteria, viruses, and fungi.

What Is Good Clinical Practice? [Everything About GCP]

Do you know what Good Clinical Practice is? It is a group of standards that ensures clinical trials are conducted reliably, safely,

What Regulation Apply To Medical Device Packaging

What Regulations Apply To Medical Device Packaging?

When you manufacture, import or purchase medical devices, have you ever focused on their functionality, design, or the technology they use? Do

ISO 11607 – Packaging for Terminally Sterilized Medical Devices

In the global world of medical devices, packaging plays a major role in making sure that the safety and effectiveness of the

What Is ISO 15189 And Why Is It Important?

Imagine your medical test results that are wrong. It could to misdiagnosis, delayed treatment, or unnecessary stress. So to avoid all these

What is BS ISO 7101? [Healthcare Organization Management]

Imagine you are running a business where every tiny detail matters – If YES you must understand “How safely products are made

What are the Requirements of ISO 13485?

ISO 13485 is an international standard identifying the need for a quality management system (QMS) specifically for the medical device industry. It