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On-line fda eventos

301 - FDA Insider
ter., 10 de jun., 09:00 GMT-4
301 - FDA Insider
ter., 10 de jun., 09:00 GMT-4
As vendas terminam em breve
Navigating FDA Inspections Successfully– Most Common Observation Strategies
quinta-feira às 11:00 GMT-4
As vendas terminam em breve
Navigating FDA Inspections Successfully– Most Common Observation Strategies
quinta-feira às 11:00 GMT-4
FDA Recalls - Before You Start, and After You Finish
ter., 29 de jul., 09:00 GMT-4
FDA Recalls - Before You Start, and After You Finish
ter., 29 de jul., 09:00 GMT-4
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
ter., 24 de jun., 11:00 GMT-4
FDA’s 2025 Color Additive Crackdown: What Food, Pharma & Supplement Brands
ter., 24 de jun., 11:00 GMT-4
US FDA Labeling Requirements for Medical Devices
sex., 13 de jun., 13:00 GMT-4
US FDA Labeling Requirements for Medical Devices
sex., 13 de jun., 13:00 GMT-4
The 6 Most Common Problems in FDA Software Validation and Verification
qui., 12 de jun., 13:00 GMT-4
The 6 Most Common Problems in FDA Software Validation and Verification
qui., 12 de jun., 13:00 GMT-4
WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
qua., 18 de jun., 18:00 GMT-5
WEBINAR: The Importance of FDA Clearance for your Aesthetic Laser
qua., 18 de jun., 18:00 GMT-5
US FDA'S AI Framework For Medical Devices
qua., 28 de mai., 10:00 GMT+5:30
US FDA'S AI Framework For Medical Devices
qua., 28 de mai., 10:00 GMT+5:30
As vendas terminam em breve
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
quinta-feira às 09:00 GMT-4
As vendas terminam em breve
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
quinta-feira às 09:00 GMT-4
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
qui., 3 de jul., 09:00 GMT-4
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
qui., 3 de jul., 09:00 GMT-4
How to Ace an FDA Meeting - Preparation and Conduct
qua., 28 de mai., 10:00 GMT+5:30
How to Ace an FDA Meeting - Preparation and Conduct
qua., 28 de mai., 10:00 GMT+5:30
Conducting and Documenting Robust Investigation for OOS Results
sex., 20 de jun., 13:00 GMT-4
Conducting and Documenting Robust Investigation for OOS Results
sex., 20 de jun., 13:00 GMT-4
The Future of Clinical Research: Leveraging ICH E6(R3)
qui., 31 de jul., 13:00 GMT-4
The Future of Clinical Research: Leveraging ICH E6(R3)
qui., 31 de jul., 13:00 GMT-4
Adicionado recentemente
Master The Vendor Auditing Of Your Computer Systems Regulated By FDA
qui., 29 de mai., 10:00 GMT+5:30
Adicionado recentemente
Master The Vendor Auditing Of Your Computer Systems Regulated By FDA
qui., 29 de mai., 10:00 GMT+5:30
FDA Warning Letter - Consent Decree Software Validation
qua., 28 de mai., 10:00 GMT+5:30
FDA Warning Letter - Consent Decree Software Validation
qua., 28 de mai., 10:00 GMT+5:30
Healthcare Sector Training - Therapeutics
ter., 1 de jul., 13:00 GMT-4 + 1
Healthcare Sector Training - Therapeutics
ter., 1 de jul., 13:00 GMT-4 + 1
ASQ Certified Medical Device Auditor (CMDA) Knowledge Ref. Course Sept-2025
sáb., 20 de set., 08:30 GMT-7
ASQ Certified Medical Device Auditor (CMDA) Knowledge Ref. Course Sept-2025
sáb., 20 de set., 08:30 GMT-7
Auditing and Qualifying Suppliers and Vendors Course
ter., 26 de ago., 12:00 GMT-4
Auditing and Qualifying Suppliers and Vendors Course
ter., 26 de ago., 12:00 GMT-4
Avoid Warning Letters in View of the U.S. FDA's Stated Goal
ter., 27 de mai., 10:00 GMT+5:30
Avoid Warning Letters in View of the U.S. FDA's Stated Goal
ter., 27 de mai., 10:00 GMT+5:30
Adicionado recentemente
Validation Of Artificial Intelligence (AI), Machine Learning (ML)
sex., 30 de mai., 10:00 GMT+5:30
Adicionado recentemente
Validation Of Artificial Intelligence (AI), Machine Learning (ML)
sex., 30 de mai., 10:00 GMT+5:30

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