Home » Medical Devices & Diagnostics » [WEBINAR] Medical Device Lunch Briefing: FDA 483 Response Best Practices
[Watch] No Surprises: Improving Medical Devices Due Diligence
Donna Godward and Dr. Janet Vargo recently presented a lunch briefing on improving medical devic...
Virtual Development Teams
Trial Master File Remediation
Patient Outreach Program Audits
Flexible, On-Demand Talent Clinical Development
Flexible, On-Demand Talent Regulatory Affairs
Clinical Trial Management System Reconciliation
Clinical Data Integrity Remediation
Blinded Data Review
How Smart Biotechs Scale Organizations Fast and Maximize Value
Virtual Pharma R&D: Open for Business
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.
[WEBINAR] Leveraging Evolving Regulatory Landscape to Accelerate Drug & Device Development
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.
YourEncore Regulatory Affairs Overview
YourEncore Clinical Development Overview
YourEncore Regulatory Affairs Handout
YourEncore Clinical Development Handout