WPC ETA Certification – Must for Wireless Medical Device
Introduction: Medical devices incorporating wireless technologies require WPC Equipment Type Approval (ETA) certification to be imported or sold in India. […]
The Vital Role of Post-Marketing Surveillance for Medical Devices
Introduction: The use of medical devices has improved healthcare enormously. However, like any technology, medical devices also carry risks. These
Medical Device Labelling: Ensuring Clarity and Safety
Introduction: In the world of healthcare, medical devices play a crucial role in diagnosis, treatment, and patient care. At the
Medical Device Grouping: An Effective Regulatory Approach
Introduction : In the dynamic world of medical devices, regulations play a critical role in ensuring patient safety and product
Understanding the Validity and Renewal of CDSCO Medical Device Import License
Introduction : As per the Medical Device Rule, 2017, the medical device import license in India needs to be renewed
Transitioning to Full Licensing: Class C and D Medical Devices in India
Introduction: On April 12, 2023, the Central Drugs Standard Control Organization (CDSCO) of India released a circular reminding Indian manufacturers and importers
Understanding Post-Approval Changes in Medical Devices: A Comprehensive Guide
Introduction : The introduction of a medical device into the market is a complex process that starts with necessary approval
New Medical Device Rules in India: Registration Certificate for Sale
The Indian medical device industry is currently experiencing a significant transformation with the Ministry of Health and Family Welfare (MoHFW) introducing
Registration Process for Class A Non-Sterile and Non-Measuring Medical Devices in India | An Overview
Medical devices play a crucial role in maintaining the health and well-being of people. The number of medical devices on