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Friday, Jan. 17th, 2025
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TRAINING DETAILS
Course : Mastering Root Cause Analysis, CAPA, and Effectiveness Checks: Practical Tools for Sustainable Solutions
Participate Type : unlimited
Course quantity : 1
Course : Mastering FDA 510(k) and PMA Submissions: A 3-Hour Virtual Seminar for Faster Approval
Participate Type : unlimited
Course quantity : 1
Course : Mastering Verification vs. Validation: Ensuring Compliance for Products, Processes, and QMS Software
Participate Type : single
Course quantity : 1
Course : Navigating FDA 510(k) Submissions: How to Sidestep Common Mistakes and Ensure Approval
Participate Type : single
Course quantity : 1
Course : Fast-Track FDA Approvals: Mastering NDAs, INDs, and Drug Manufacturing Standards
Participate Type : single
Course quantity : 1