From vascular stents to dental implants, many medical devices work by being temporarily or permanently placed in the human body. This necessitates rigorous testing of their safety and performance in nonclinical animal models. However, the guidelines and regulatory requirements are not always easy and straightforward to interpret for medical device studies.

In this webinar brought to you by Inotiv, Maria Bates and Nicolette Jackson will discuss how to navigate the regulatory landscape and enhance medical device development by leveraging pathology insights

What You’ll Learn:

• Key criteria for comprehensive nonclinical surgical and medical device evaluation
• Fulfilling regulatory submission requirements for medical device programs
• How integrating pathology studies can enhance device safety and effectiveness
• The benefits of connectivity between in-life facilities, histology, and pathology

Perfect for professionals involved in medical device development!

Register

1:00 PM – 2:30 PM Eastern Time