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NAMSA Webinar: Do’s and Dont’s for Early-Stage IVD Product Development and Risk Mitigation
April 22 @ 11:00 am - 12:00 pm
Join BioOhio member NAMSA on April 22 for the webinar Do’s and Dont’s for Early-Stage IVD Product Development and Risk Mitigation.
A well-planned approach to navigate the early stages of In Vitro Diagnostic (IVD) development will yield significant competitive advantages by shortening time-to-market without additional costs. Robust plans that include factors such as market opportunities, regulatory requirements and demonstration of product safety/efficacy can effectively impact development timelines and costs.
Join NAMSA for this webinar and discover how to navigate a variety of scenarios to gauge time and cost-to-market. This online event will also review the U.S. FDA’s latest guidelines regarding the conduct of trials during the COVID-19 pandemic and decode some of the effective pathways and come up with an optimal approach.
Participants of this webinar will leave with a better understanding of:
How a start-up to mid-size IVD manufacturer can reduce the risk in product development cycle
How to effectively shorten the time-to-market and secure a competitive advantage
Strategic areas of importance within the product development lifecycle where careful planning is required
How to plan for clinical trials and product development under COVID-19 pandemic
Where a company should invest its resources when planning for a new IVD product