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Events fda online

How to Prepare for an FDA Inspections?
Di., 15. Juli, 13:00 GMT-4
How to Prepare for an FDA Inspections?
Di., 15. Juli, 13:00 GMT-4
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AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
heute um 11:00 GMT+5:30
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AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
heute um 11:00 GMT+5:30
Risk Management for AI in Medical Devices – FDA’s TPLC Management Draft
Mi., 30. Juli, 13:00 GMT-4
Risk Management for AI in Medical Devices – FDA’s TPLC Management Draft
Mi., 30. Juli, 13:00 GMT-4
Responding to a Form 483 Citation and/or Warning Letter Issued by FDA
Fr., 27. Juni, 13:00 GMT-4
Responding to a Form 483 Citation and/or Warning Letter Issued by FDA
Fr., 27. Juni, 13:00 GMT-4
Preparing a FDA 510(k) submission - What to Know in 2025
Do., 26. Juni, 13:00 GMT-4
Preparing a FDA 510(k) submission - What to Know in 2025
Do., 26. Juni, 13:00 GMT-4
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
Di., 24. Juni, 11:00 GMT-4
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
Di., 24. Juni, 11:00 GMT-4
Navigating FDA Inspection Most Common Observation and Prevention Strategies
Mi., 9. Juli, 11:00 GMT-4
Navigating FDA Inspection Most Common Observation and Prevention Strategies
Mi., 9. Juli, 11:00 GMT-4
Cybersecurity - The Latest US FDA Requirements
Di., 24. Juni, 13:00 GMT-4
Cybersecurity - The Latest US FDA Requirements
Di., 24. Juni, 13:00 GMT-4
Medical Device Software Validation that Meets FDA Requirements
Di., 29. Juli, 13:00 GMT-4
Medical Device Software Validation that Meets FDA Requirements
Di., 29. Juli, 13:00 GMT-4
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WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
Mittwoch um 18:00 GMT-5
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WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
Mittwoch um 18:00 GMT-5
Medical Device Non-Product Software Validation Training
Di., 8. Juli, 13:00 GMT-4
Medical Device Non-Product Software Validation Training
Di., 8. Juli, 13:00 GMT-4
Master Validation Plan - The Unwritten Requirements Course
Mi., 9. Juli, 11:00 GMT-4
Master Validation Plan - The Unwritten Requirements Course
Mi., 9. Juli, 11:00 GMT-4
Evolution of US Drug Label Management: Leveraging Structured Product
Mi., 6. Aug., 15:00 GMT-4
Evolution of US Drug Label Management: Leveraging Structured Product
Mi., 6. Aug., 15:00 GMT-4
21 CFR Part 11, FDAs Guidance for Electronic Records & Electronic Signature
Mittwoch um 13:00 GMT-4
21 CFR Part 11, FDAs Guidance for Electronic Records & Electronic Signature
Mittwoch um 13:00 GMT-4
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Do., 3. Juli, 09:00 GMT-4
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Do., 3. Juli, 09:00 GMT-4
US FDA'S AI Framework For Medical Devices
Mi., 28. Mai, 10:00 GMT+5:30
US FDA'S AI Framework For Medical Devices
Mi., 28. Mai, 10:00 GMT+5:30
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Conducting and Documenting Robust Investigation for OOS Results
Freitag um 13:00 GMT-4
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Conducting and Documenting Robust Investigation for OOS Results
Freitag um 13:00 GMT-4
Drug, Device and Combination Product Development.
Fr., 27. Juni, 13:00 GMT-4
Drug, Device and Combination Product Development.
Fr., 27. Juni, 13:00 GMT-4
FDA Regulation For Over-The-Counter (OTC) Drug Products
Mi., 4. Juni, 10:00 GMT+5:30
FDA Regulation For Over-The-Counter (OTC) Drug Products
Mi., 4. Juni, 10:00 GMT+5:30
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Analytical Methods Validation - ICH Q14 Overview for Regulatory Approval
Mo., 23. Juni, 11:00 GMT+5:30
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Analytical Methods Validation - ICH Q14 Overview for Regulatory Approval
Mo., 23. Juni, 11:00 GMT+5:30

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