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The Going Global: Best Practices Online Seminar Series These free, regularly-scheduled, 60-minute seminars are designed and facilitated by clinivation experts to provide you with the knowledge, process, and best practices to build robust submissions and manage families of worldwide approvals.
 These seminars frequently include distinguished panelists and participants from regulatory agencies worldwide. Clinivation is a Regulatory Affairs Professionals Society (RAPS) RA Professional Development Portal provider. Clinivation is committed to enhancing the ongoing professional development of regulatory affairs professionals and other stakeholders through appropriate regulatory affairs learning activities and programs. Clinivation has agreed to follow RAPS-established operational and educational criteria. Each Going Global: Best Practices Online Seminar Series presentation has been pre-approved by RAPS as eligible for 1 hour of Continuing Education credit towards a participant's RAC recertification upon full completion. The target audience includes regulatory affairs and quality engineering managers and executives in the medical device industry.
Past Seminar Presentations Available View
We're glad to share these Going Global: Best Practices Online Seminar Presentations with our industry colleagues.
A comprehensive list of past seminar topics and presentations is available to view and download on the Seminar Presentations section of our website. Are you a Frequent Filer? Register for a Live, Online Demo
Learn how to take the time and labor out of managing your worldwide medical device approvals. With clinivation Global® software, now you can access everything you need to build and track all of your submissions and registrations.
Register now to schedule a live online demonstration of clinivation Global. Request Information
For more information, contact clinivation at 508.655.6560,
via email at solutions@clinivation.com,
or request a live demo.
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