Are You Reg. Ready? Getting Your Medical Affairs Team Primed to Manage New Regulatory Requirements

There’s been plenty of discussion on the submission scope of current EU MDR and pending EU IVDR regulatory requirements for medical device manufactures. But what of organizational change management readiness? How should a medical device organization’s different business functions collaborate and align their people, processes, and knowledge to meet these regulatory requirements effectively and efficiently? Join us for a behind-the-scenes look at how one company is managing change within their organization.