How a Regulatory Strategy Report Can Help in Medical Device Introduction in India
The Indian medical device market is advancing rapidly and is currently valued at approximately USD 12 billion, which is expected […]
A Guide to Legal Metrology Compliance for Medical Devices in India
In India, the manufacturing, sale, and distribution of medical devices are subject to stringent regulatory requirements designed to ensure that
A Comprehensive Guide on “Non-Conviction Certificate” for Medical Devices
In India, the manufacture, import, and distribution of medical devices are regulated by the Central Drugs Standards Control Organization (CDSCO)
Insight into the Medical Devices Market in India
Over the last decade, the medical device industry in India has experienced remarkable growth, driven by increasing demand for a
Registration of Cosmetics in India
Cosmetics are utilized to improve a person’s appearance. These are used for various beauty treatments such as skin tightening, hair removal,
Materiovigilance Programme of India (MvPI) :DCGI Calls for Strengthening Medical Device Adverse Event Reporting
The Drugs Controller General of India (DCGI) has called for the timely reporting of adverse events related to medical devices by issuing
Intraocular Lenses and Regulatory Processes
Intraocular Lenses (IOLs) are special lenses put inside the eye during surgery to replace the natural lens. This often happens when
CDSCO Update: New Online PSUR Guidelines in India
The Central Drug Standard Control Organization (CDSCO) has recently made a change to how safety reports for medical devices and in-vitro diagnostic
CDSCO Test License for Medical Devices in India
Chapters IV and V of the MDR 2017 provide detailed guidelines for manufacturers and importers seeking to manufacture or import small quantities of medical devices for