FDAnews Announces — Sustained Medical Device Regulation Compliance: Ensure Your Regulatory Processes and Tools are Fully Optimized, Sponsored by Instem, Webinar, May 20

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Free Webinar: Optimize Regulatory Processes that will Comply with EU-MDR/IVDR

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WCG FDAnews

Sustained Medical Device Regulation Compliance:
Ensure Your Regulatory Processes and Tools are Fully Optimized
A Free FDAnews Webinar, Sponsored by Instem
Wednesday, May 20, 2020, 1:30-2:30 p.m. EDT
http://info.fdanews.com/sustained-medical-device-regulation-compliance?free_webinar_source=HP

Even though the European Commission will likely postpone the date of application for the European Medical Device Regulation (EU-MDR), the medical device industry must not curtail compliance readiness activities.

Implementation of EU-MDR and IVDR will exponentially increase the volume and velocity of data that requires regulatory operations support. Now is the time to challenge the status quo and leverage technology solutions to improve the efficiency of regulatory operations information management.

Attend this free webinar sponsored by Instem and understand how to optimize processes and tools to ensure that regulatory operations meet global regulatory compliance.

Kim Young, Instem’s Director, Global Regulatory Intelligence, and Chris Nichols, an Instem Product Specialist, will explain the critical steps of confirming MDR readiness and remaining compliant with the new regulation. They’ll share how Regulatory Information Management (RIM) software can reduce several weeks of manual efforts into just a few hours — if not minutes.

Gain insights into:

  • How challenges are contrary to the way regulatory teams have traditionally operated across the industry… and how to overcome them
  • How to integrate the critical aspects of EU-MDR compliance, and what one must consider to deploy a sustainable compliance framework
  • How technology is optimizing some of the largest regulatory operations teams by helping them rationalize their efforts between rote tasks and business-critical strategic endeavors
  • How to avoid suffering undue challenges for want of the right technology and tools
  • How to develop a sustainable cadence to meet global compliance requirements, which will require a serious modernization of processes, technologies and tools

When one understands how to implement true end-to-end regulatory operations automation, one will ensure compliance with EU-MDR.

Webinar Details:
Sustained Medical Device Regulation Compliance:
Ensure Your Regulatory Processes and Tools are Fully Optimized
A Free FDAnews Webinar, Sponsored by Instem
Wednesday, May 20, 2020, 1:30-2:30 p.m. EDT
http://info.fdanews.com/sustained-medical-device-regulation-compliance?free_webinar_source=HP

Easy Ways to Register:
Online: http://info.fdanews.com/sustained-medical-device-regulation-compliance?free_webinar_source=HP
By phone: 888.838.5578 or 703.538.7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations

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Michelle Butler
FDAnews
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