A Comprehensive Guide to Cybersecurity for Medical Devices and IVDs […] A Comprehensive Guide to Cybersecurity for Medical Devices and IVDs Read More »
Testing and Evaluation of Medical Devices and IVDs – CDSCO Circular Testing and Evaluation of Medical Devices and IVDs – CDSCO Circular Read More »
MHRA to Recognize Medical Devices from EU, US, Canada, and Australia MHRA to Recognize Medical Devices from EU, US, Canada, and Australia Read More »
The Vital Role of Plastic Molding in Disposable Medical Devices The Vital Role of Plastic Molding in Disposable Medical Devices Read More »
Navigating 21 CFR Part 820: Compliance and Requirements for Medical Device Manufacturers Navigating 21 CFR Part 820: Compliance and Requirements for Medical Device Manufacturers Read More »
CDSCO Urges Medical Device Firms to Pay Retention Fees to Avoid License Cancellations CDSCO Urges Medical Device Firms to Pay Retention Fees to Avoid License Cancellations Read More »
Disposable Plastic Syringe Registration Process (USFDA, European CE, SFDA and Other Regulatory Countries) Disposable Plastic Syringe Registration Process (USFDA, European CE, SFDA and Other Regulatory Countries) Read More »
Continuation of Import and Manufacturing for Class C & D Medical Devices: Regulatory Update Continuation of Import and Manufacturing for Class C & D Medical Devices: Regulatory Update Read More »
Indian Government Strengthens Medical Device Safety with New Reporting Mandate Indian Government Strengthens Medical Device Safety with New Reporting Mandate Read More »
The Essential Requirements for Software as a Medical Device (SaMD Compliance) The Essential Requirements for Software as a Medical Device (SaMD Compliance) Read More »