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Webinar: FDA Considerations to Fast-track your Translational Research
January 13, 12:00 pm to 1:00 pm
The bench-to-bedside translation of innovative drug therapies and medical devices continues to transform the future of healthcare. Understanding the regulatory requirements and expectations of drug and device development allows for the design of more efficient, yet comprehensive, clinical protocols and a faster path to the bedside.
In this session, two leaders from the industry will discuss the basics of FDA regulations pertinent to therapeutics and medical devices. They will share key elements that early-stage innovators should consider throughout the developmental pipeline, including early bench research and preclinical studies.
This is an online event; please register to receive Zoom access credentials. All Penn State faculty, staff and students are invited to attend.