Medical Device – DSI InPharmatics

June 1, 2022

Published by Meranda Parascandola at June 1, 2022

Virtual Audits: How to Provide Objective Evidence to Support Quality Medical Devices

Audits are necessary. However, just as we learned during the COVID-19 pandemic, that many people could perform their jobs perfectly well without getting in their car or on a train to come to the office, we have also seen that many audits can be done well…virtually. There is a place for both virtual and on-site audits.

June 7, 2022

Published by Meranda Parascandola at June 7, 2022

FDA-Required Medical Device Regulations

Medical devices have been saving lives for decades. And medical devices are quickly changing as new technology such as 3D printing, software, hardware and algorithms are being incorporated into device designs. Medical devices are not simply band aids and thermometers any longer. They are sophisticated designs that help people with a myriad of problems and in many cases, they prolong and save lives.

August 8, 2022

Published by Meranda Parascandola at August 8, 2022

How Global Regulatory Strategies Create Pathways for Medical Devices

You've likely heard the phrase “time is money.” No other statement could be more accurate for the medical device industry. Each day your company is not approved to market your device is not only a day of lost revenue, but a day patients don’t get to benefit from the value […]