Virtual Webinar

Understanding how Business Operations + FDA Regulations Overlap

In addition to starting and running a typical manufacturing business, MedTech products have additional regulatory requirements such as Quality Management systems, development phases, risk management, document control, and design controls.

In this webinar we’ll provide an overview of the typical MedTech development process, overlaid on a traditional manufacturing business lifecycle. We will also identify how business and MedTech product development workstreams interplay.

In the startup world, we rarely have the luxury of managing one simple project at a time. Join us and learn how to use the overlap strategically to keep your business on track!

Register HERE