Home » Medical Devices & Diagnostics » [WEBINAR] State of the Industry Webinar: U.S. Regulatory Policy Improvements
The Frontiers of Rare Disease Development: Advances in Regulatory Science with Dr. Tim Franson (Ep. 18 of The Pharmcast)
This week on The Pharmcast, we catch up with Dr. Tim Franson to discuss the leading edge of...
How Smart Biotechs Scale Organizations Fast and Maximize Value
Virtual Development Teams
A Kickstart for Your Development Programs
Joseph Lamendola, PhD and Timothy Franson, MD walk through the requirements for kickstarting a new development program in a Biopharma organization.
Trial Master File Remediation
Leveraging the Evolving Regulatory Landscape to Accelerate Drug & Medical Devices Development
The Food & Drug Administration has actively engaged in efforts to issue new regulations and guidance aimed at driving innovation, reducing risk, and improving patient safety.
Patient Outreach Program Audits
[WEBINAR] Leveraging Evolving Regulatory Landscape to Accelerate Drug & Device Development
Flexible, On-Demand Talent Clinical Development
How Blockchain is Revolutionizing the World and Changing Healthcare as We Know It (Ep. 20 of The Pharmcast)
In this episode of The Pharmcast, we join YourEncore Expert, Darryl Glover, to discuss one of the hottest technologies on the market today: blockchain. We've heard some people...
Flexible, On-Demand Talent Regulatory Affairs
MD&D Expert Webinar
Clinical Trial Management System Reconciliation
Clinical Data Integrity Remediation
Blinded Data Review
YourEncore Project Spotlight:Global Analysis and Optimization
Ten Tips for Enterprise Technology Adoption in Pharma
The RFP processes are robust, the ROI models are compelling, the software is best of breed, and the expectations are high. So, why do so many software deployment programs in Pharma fail...
[WEBINAR] Drug-Device/Diagnostics Combination Products: Understanding the Rapidly Changing Landscape