Understanding Medical Device Regulatory Pathways – 510(k), PMA & Exemptions
Feb 04, 2026
01 : 00 PM
5S for Operators and Human Error Reduction
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Human Error Solutions: How we Reduced 60% of Human Errors in Less Than a Year, a Case Study
Jan 20, 2026
How to Write SOPs (Procedures) for Human Error Reduction/ Prevention
Jan 13, 2026
101_Human Error Reduction in GMP Manufacturing/Floor
Dec 12, 2025
Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance
Dec 01, 2025
Pharma 4.0: Next Generation Technology Approach to GxP Products, Systems, Data, & FDA Compliance
Nov 30, 2025
Medical Device Software Validation Meeting: FDA Regulations
Nov 29, 2025
T&C Applicable T&C
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