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How to Prepare for an FDA Inspections?
mar. 15 juil., 17:00 UTC
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How to Prepare for an FDA Inspections?
mar. 15 juil., 17:00 UTC
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AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
mardi prochain à 05:30 UTC
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AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
mardi prochain à 05:30 UTC
Risk Management for AI in Medical Devices – FDA’s TPLC Management Draft
mer. 30 juil., 17:00 UTC
Risk Management for AI in Medical Devices – FDA’s TPLC Management Draft
mer. 30 juil., 17:00 UTC
Preparing a FDA 510(k) submission - What to Know in 2025
jeu. 26 juin, 17:00 UTC
Preparing a FDA 510(k) submission - What to Know in 2025
jeu. 26 juin, 17:00 UTC
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
mar. 24 juin, 15:00 UTC
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
mar. 24 juin, 15:00 UTC
Navigating FDA Inspection Most Common Observation and Prevention Strategies
mer. 9 juil., 15:00 UTC
Navigating FDA Inspection Most Common Observation and Prevention Strategies
mer. 9 juil., 15:00 UTC
Cybersecurity - The Latest US FDA Requirements
mar. 24 juin, 17:00 UTC
Cybersecurity - The Latest US FDA Requirements
mar. 24 juin, 17:00 UTC
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FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality
demain à 17:00 UTC
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FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality
demain à 17:00 UTC
Medical Device Software Validation that Meets FDA Requirements
mar. 29 juil., 17:00 UTC
Medical Device Software Validation that Meets FDA Requirements
mar. 29 juil., 17:00 UTC
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WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
mercredi prochain à 23:00 UTC
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WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
mercredi prochain à 23:00 UTC
Medical Device Non-Product Software Validation Training
mar. 8 juil., 17:00 UTC
Medical Device Non-Product Software Validation Training
mar. 8 juil., 17:00 UTC
Master Validation Plan - The Unwritten Requirements Course
mer. 9 juil., 15:00 UTC
Master Validation Plan - The Unwritten Requirements Course
mer. 9 juil., 15:00 UTC
Evolution of US Drug Label Management: Leveraging Structured Product
mer. 6 août, 19:00 UTC
Evolution of US Drug Label Management: Leveraging Structured Product
mer. 6 août, 19:00 UTC
21 CFR Part 11, FDAs Guidance for Electronic Records & Electronic Signature
mercredi prochain à 17:00 UTC
21 CFR Part 11, FDAs Guidance for Electronic Records & Electronic Signature
mercredi prochain à 17:00 UTC
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
jeu. 3 juil., 13:00 UTC
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
jeu. 3 juil., 13:00 UTC
US FDA'S AI Framework For Medical Devices
mer. 28 mai, 04:30 UTC
US FDA'S AI Framework For Medical Devices
mer. 28 mai, 04:30 UTC
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Conducting and Documenting Robust Investigation for OOS Results
vendredi prochain à 17:00 UTC
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Conducting and Documenting Robust Investigation for OOS Results
vendredi prochain à 17:00 UTC
Drug, Device and Combination Product Development.
ven. 27 juin, 17:00 UTC
Drug, Device and Combination Product Development.
ven. 27 juin, 17:00 UTC
FDA Regulation For Over-The-Counter (OTC) Drug Products
mer. 4 juin, 04:30 UTC
FDA Regulation For Over-The-Counter (OTC) Drug Products
mer. 4 juin, 04:30 UTC
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Analytical Methods Validation - ICH Q14 Overview for Regulatory Approval
lun. 23 juin, 05:30 UTC
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Analytical Methods Validation - ICH Q14 Overview for Regulatory Approval
lun. 23 juin, 05:30 UTC

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