Post-Market Surveillance (PMS) in India : A Global Comparison with Europe and the U.S. FDA

When a medical device or in-vitro diagnostic (IVD) enters the market, regulatory approval is only the beginning. The true test lies in how the device performs in real-world conditions. That’s where Post-Market Surveillance (PMS) steps in. PMS acts as the backbone of patient safety, ensuring that any risks are detected early, corrective actions are taken […]