Associate Director - Head of Device Development and Support
ALK A/S
Tine Albeck serves as Senior QA at ALK A/S, Denmark, overseeing quality for drug-delivery devices and combination products. She led ALK’s ISO 13485 certification and MDR compliance, specializing in design control implementation and CMO oversight. An experienced ISO 13485 auditor, she holds a Master’s in Medical Engineering from Danish Technical University.
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Workshop: Unlocking Best Practices for Sponsors and Regulators in Combination Product Submissions
Wednesday, November 12, 2025
12:30 PM - 3:00 PM East Coast USA Time
Thursday, November 13, 2025
8:20 AM - 9:05 AM East Coast USA Time
Clinical Investigations for Combined Use Systems
Thursday, November 13, 2025
11:25 AM - 12:25 AM East Coast USA Time