After years of development, it’s time to communicate a positive benefit-risk that can support approval of a regulatory submission.
Toronto, ON (PRWEB) October 10, 2019
Join Kell Cannon, Founding Partner & Scientific Lead at 3D Communications in a live webinar on Wednesday, October 23, 2019 at 12pm EDT (5pm BST/UK) to hear about a practical, comprehensive, step-by-step method to ensure you and your team are prepared for your FDA submission. Kell brings 20 years of leadership at some of the world’s largest pharmaceutical companies along with a decade of healthcare consulting experience to help clients achieve regulatory success and communicate product value.
After years of development, it’s time to communicate a positive benefit-risk that can support approval of a regulatory submission. Clearly, no clinical development program is perfect; addressing and overcoming barriers is essential to regulatory success. In this free webinar, hear about a practical, comprehensive step-by-step method to ensure you and your team are prepared to:
- Maximize the credibility of how you’re interpreting your data;
- Proactively identify and address gaps, limitations and concerns;
- Align your team’s goals and messaging across the submission document; and
- Enhance your interactions with regulatory agencies
This webinar will be useful to anyone working in the pharmaceutical, biologics and medical device industries who is contributing to interpreting and communicating the clinical data within the integrated analyses and benefit-risk overview within your submission.
For more information or to register for this event, visit Winning From the Beginning: Best Practices to Increase Your Chances for First-Pass Approvals in Key Markets.
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