How Regulatory Changes Can Impact Product Development

How Regulatory Changes Can Impact Product Development

The MedTech global regulatory landscape is evolving.

Is your organization ready?

Regulatory and Product Development departments need to do more than cooperate —they need to be working hand in hand. Having a strong regulatory strategy from the beginning of development helps you:

  • Establish a clear pathway to market
  • Make better and more informed decisions
  • Outline critical requirements to all development and business teams
  • Prevent delays, regulatory warnings, and loss of profitability

In this webinar, Director of Regulatory and Clinical Affairs, Carrie Hetrick, and other industry experts discuss how to help your team produce synergistic results.

Carrie’s insight was part of the event, Global MedTech Regulatory Trends: True Quality Summit Series presented by Greenlight Guru.

Watch the Regulatory & Product Development: Relationship Counseling Course now.

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Dan Sterling Photo of Dan Sterling President
250 Moonachie Rd., Suite 400 Moonachie, NJ 07074
201-227-7569 dan@sterlingmedicaldevices.com
John Campbell Photo of John Campbell VP of Operations
250 Moonachie Rd., Suite 400 Moonachie, NJ 07074
201-227-7569 jc@sterlingplm.com
John Fargo Photo of DanJohn Fargo PLM Manager
250 Moonachie Rd., Suite 400 Moonachie, NJ 07074
201-227-7569 jf@sterlingplm.com