Building Sustainable Ways of Maintaining a Solid Regulatory Strategy
Thursday, March 7, 2024
11:45 AM – 12:45 PM East Coast USA Time
Location: Concourse C/D
With rapidly evolving regulatory and market demands, regulatory compliance teams are always under pressure to do more with less, requiring a fundamental shift in operations, systems, and processes. So how do you build a sustainable way of maintaining a solid regulatory strategy that can withstand all and any change that the organization faces? A recent survey of nearly 100 global device and diagnostics organizations gathered insights to better understand the industry’s progress towards driving a sustainable work environment that impacts regulatory, but also other cross functional partners. The survey reviled that MedTech companies still use manual processes, disconnected data, and siloed systems that are neither scalable nor flexible, preventing them from taking advantage of what is in front of them.
A case study with a MedTech industry leader representative will illustrate how to transform to a sustainable regulatory strategy.
Learning Objectives:
Upon completion of this session, participants should be able to:
Identify what a solid, lasting regulatory strategy looks like and how to achieve it.
Discuss best practices with peers on developing regulatory processes that are built for change.
Understand how to best integrate cross domain workflows into a regulatory process
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