Access our on-demand webinar.
From vascular stents to dental implants, many medical devices require rigorous testing in nonclinical animal models to ensure their safety and efficacy. However, understanding the specific guidelines and regulatory requirements can be challenging. In this webinar, Dr. Maria Bates and Dr. Nicolette Jackson from Inotiv provide valuable insights into navigating the regulatory landscape and enhancing medical device development.
Our experts discuss:
- Understanding regulatory requirements: Learn about the specific guidelines and standards that apply to medical device studies.
- Leveraging pathology insights: Discover how pathology can provide critical information for assessing device safety and performance.
- Enhancing medical device development: Explore strategies for optimizing device design and manufacturing processes based on pathology findings.
- The importance of interdepartmental connectivity: Understand how effective communication and collaboration between in-life facilities, histology, and pathology can streamline the development process.
Complete the form to access this on-demand webinar and gain valuable insights to accelerate your medical device development efforts.
