Managing Global Regulatory Strategy and Compliance: Assessing Status, Gaps, and Needs

Join us for an engaging discussion where industry leaders will share key insights and findings from a recent survey conducted with Medtech Intelligence. This webinar will explore the top challenges and opportunities in the medical device industry, discuss planned investments for the near and long term, and provide guidance on aligning with evolving regulatory requirements. Topics will include identifying regulatory gaps, risk mitigation strategies, and leveraging technology and resources to enhance compliance.

Don’t miss this opportunity to enhance your regulatory skills and understanding.

Webinar Speakers

  • 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.

  • Gregory Jacobson: Sales Director, Medical Devices, SGS North America Inc.

Gain actionable knowledge and insights with our webinar:

  • Identify Regulatory Gaps: Understand why gaps in regulatory intelligence and compliance processes are overwhelming for teams and organizations.

  • Risk Mitigation: Learn strategies to mitigate risks associated with the growing complexities of global regulatory compliance.

  • Focus Areas: Discover where to prioritize MDR/IVDR efforts and investments.

  • Technology and Resources: Explore technologies and resources for cost-effective management of current bandwidth limitations in the industry.
Are you seeking assistance with a regulatory compliance need?

Please complete the form below to outline your medical device/pharmaceutical/IVD regulatory support requirements. Our team will promptly review your submission and reach out to confirm a consultation time. Thank you for your interest.

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