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FDA Compliance for Mobile Applications

21 CFR Part 11 – Compliance for Electronic Records and Signatures

4-Hour Virtual Seminar on Risk Assessment Techniques & Tools in the Medical Device industry

4-Hour Virtual Seminar on Risk Assessment Techniques & Tools in the Medical Device industry

Effective CAPA – How the FDA Investigates Your CAPA System?

Excel Spreadsheets: Ensuring Data Integrity and 21 CFR Part 11 Compliance

CAPA – How the FDA Investigates Your CAPA System

ISO 13485: Medical Device Quality Management Systems

Excel Spreadsheets: Ensuring Data Integrity and 21 CFR Part 11 Compliance

Excel Spreadsheet Validation for Part 11 to Eliminate 483s