MDR Labelling Requirements for Medical Devices in India
Medical device labelling is essential for conveying vital information related to the medical device. The labels guide users, thereby play a pivotal role in patient safety. Medical devices are one of the pillars of the healthcare industry. Regulatory guidelines are in...
CDSCO Registration for Defibrillators in India
Defibrillators are lifesaving medical devices for emergency situations. With the rise in sudden cardiac arrest incidences in India, defibrillators are in high demand. Medical device companies are viewing this increased demand as a potential business option. With...
CDSCO Regulations for Dialysis Machine Manufacturing in India
In the recent past, there has been an increasing prevalence of chronic and acute kidney failure incidences in India. Dialysis treatment can help improve the quality of life of these patients. However, owing to the paucity of low-cost dialysis machines in India, most...
CDSCO Loan License for Medical Devices
The Medical Devices Act of 2017, provides a regulatory framework governing medical devices marketed in India. The regulations ensure safe, effective, and high-quality medical devices enter the market. This ensures medical devices meeting certain quality benchmark are...