IMARC Research has published a whitepaper outlining the similarities and differences between drug and device clinical trials. Since IMARC focuses primarily in the medical device space, we felt it was important to highlight the differences between the two trials. It has proven to be one of our more popular whitepapers, so we have decided to offer an infographic as a quick reference.
Clearly, the process of getting a drug or device approved is different, but both require an ethical commitment combined with the proper controls and an understanding the differences – in the details – between drugs and devices. Understanding these similarities and appreciating the differences is important for clinical researchers who are involved in both drug and device trials.
So while the investigations of drugs and devices have their differences, by design these differences are intended to accomplish the game goal: to safeguard research participants while bringing safe and effective products to the market as quickly as possible.
Please take time to download IMARC’s infographic: Comparing Drugs & Devices: How are the Clinical Trials Regulated?
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.