Virtual Webinar with Florida Atlantic University

About the Webinar

Join Mamta Puri-Lechner, Ph.D., and Kanchana Iyer, Senior Consultants at Halloran Consulting Group, for an insightful webinar on the essential regulatory considerations for drug, biologic, and medical device development. This session will provide a high-level overview of how to determine product classifications, effectively navigate regulatory pathways, and ensure compliance with agency expectations.

Key topics include understanding the critical differences between drug, device, and combination product submissions, developing a global regulatory strategy, and planning for both pre- and post-market approval activities. The speakers will share best practices for designing medical devices with safety and usability in mind, as well as provide practical tips for early-stage companies looking to align with regulatory agencies and secure market approval.

Whether you are in early development or preparing for product launch, this webinar will offer valuable insights into regulatory requirements, risk management strategies, and the considerations needed for a successful product journey from concept to commercialization.

Don't miss out on this opportunity to hear from industry experts and gain actionable knowledge to accelerate your product's path to market.