Event Ended

Quality and Regulatory pathways for SaMD and AI devices

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By Eventura World

Rev Content Session: Filing Deadlines, Tax, and Regulatory Obligations
Fri, Jan 16, 2026 12:00 PM EST (-05:00)
Free
Excellence in Documentation Practices and Regulatory Compliance (FDA & EMA)
Thu, Jan 8, 2026 1:00 PM EST (-05:00)
Free
Mastering Biosimilar Development: A Comprehensive Guide to Regulatory
Wed, Jan 28, 2026 3:00 PM EST (-05:00)
$149.50 - $1,794
Partnering for Innovation: UK Regulatory & Growth Opportunities
Thu, Jan 29, 2026 12:30 PM PST (-08:00)
Free
AI in Health Sciences: Regulatory and IP Considerations
Thu, Jan 29, 2026 11:30 AM EST (-05:00)
Free
Lovin’ Care in Practice: Aligning with the Regulatory Framework
Wed, Jan 21, 2026 10:00 AM GMT (+00:00)
£72
FCA Priorities for 2026: Navigating the regulatory landscape
Tue, Jan 13, 2026 9:30 AM GMT (+00:00)
£11.55
Mastering Documentation Practices and Compliance with Regulatory Standards
Thu, Jan 8, 2026 1:00 PM EST (-05:00)
Free
European Medical Device Regulation (EU) 2017/745
Tue, Jan 27, 2026 9:00 AM EST (-05:00)
$1,440 - $1,600
Medical Device Software Validation Meeting: New FDA Regulations
Fri, Jan 16, 2026 1:00 PM EST (-05:00)
$214.19 - $374.25