GET CERTIFIED AS A CRDMCP
Successful completion of these three training sessions is intended to meet the needs of individuals who are either new to biopharmaceutical-based document management, Information Management, and regulatory submission publishing for health authorities, or already experienced in one area and looking to gain a broader understanding of the full continuum of regulated document and submission production activities. Understanding the various steps throughout the life of document components from their conception, publishing into a submission, delivery to regulatory agencies, and ultimate company archival will result in a comprehensive knowledge foundation for attendees from all functional areas along the life-span of regulatory content.
This webinar package is offered on-demand. With your purchase, you may view all three previously recorded sessions at your convenience. Access to the on-demand webinars will be made available via email within 1 business day after your purchase.
Your registration entitles you to one log-in per course. Course testing capabilities, stored results for training records, and completion certificates are available for only one registrant per package purchase.