Featured Product In Devices
Selecting and Implementing Electronic Document Management Systems in the EU
$197.00
Converting to an electronic document management system (eDMS) is key to increasing your record-keeping efficiency. Only one resource enables you to do that in a cost-effective manner while ensuring compliance with EU regulations: Selecting and Implementing Electronic Document Management Systems in the EU. Read More
Devices
FDA Pathways to Bring your Medical Device to Market: What Regulatory Professionals Need to Know – Webinar Recording/Transcript
$287.00
Building a World-Class Regulatory Intelligence and Support System – Webinar Recording/Transcript
$287.00
Engaging with the FDA: Best Practices for Dealing with Warning Letters, Seizures, Injunctions — and More – Webinar Recording/Transcript
$287.00
Real-World Evidence in Medical Product Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
The FDA’s Focus on Clinical Data Integrity Throughout Product Development and Approval – Webinar Recording/Transcript
$287.00
FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers – Webinar Recording/Transcript
$287.00