WEBINAR

July 31, 2024

12:00 PM - 1:00 PM ET US

Managing global regulatory strategy and compliance: assessing status, gaps, and needs.

In a recent MTI audience survey in partnership with regulatory consulting firm, Celegence, only 6% of respondents said the regulatory expertise and compliance processes with their organizations are comprehensive. Nearly 1/3 reported adequate processes but insufficient comprehension of changing requirements. Overall, the indication is a medical device industry in need of more regulatory resources, expertise, and technology.

In this webinar, our industry panel of notified bodies, regulatory management & maintenance experts, and medical writers share details of this recent research, explore changing regulatory landscapes, identify the most critical gaps, and offer insights on knowledge, technology and resources to help improve regulatory intelligence and mitigate compliance deficits.

Learning objectives:

  • Recognize why the gaps in your regulatory intelligence and compliance processes are overwhelming you, your team and your organization.
  • How to mitigate the risks in the growing complexities of global regulatory compliance.
  • Where to focus MDR/IVDR priorities and investment.
  • Technologies and resources for cost-effective management of current bandwidth limitations being experienced across the industry.

Panelists:

Dr. Pratibha Mishra, Senior Manager – Medical Device Services, Celegence

 

Erin Cosgrove, VP, Business Development – Medical Devices, Celegence

 

Ibim Tariah, Ph.D., Technical Director, Medical Devices, SGS North America Inc.*

*SGS is a participant in this webinar for comment purposes only on information that is in the public domain. As a Notified Body, SGS cannot endorse any consulting firm and SGS’s participation in this webinar should not be construed as such.

 

 

Gregory Jacobson, Sales Director – Medical Devices, SGS North America*

*SGS is a participant in this webinar for comment purposes only on information that is in the public domain. As a Notified Body, SGS cannot endorse any consulting firm and SGS’s participation in this webinar should not be construed as such.

 

Moderated by:

Rich West, Editorial Director & Publisher, MedTech Intelligence

Who should attend:

Medical Device Leadership, Senior Product Managers, Regulatory Affairs/Quality Assurance Managers, Product Development & Design Teams, Manufacturing/Operations Leaders, Human Resources and Finance Leadership.

Please fill out registration form: