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Événements fda En Ligne

FDA Audit and Inspection Online Training Course
Thu, Feb 26, 12:00 PM EST
FDA Audit and Inspection Online Training Course
Thu, Feb 26, 12:00 PM EST
Les ventes se terminent bientôt
Inside the FDA Inspection: Managing Interviews, Requests, and FDA 483 Risk
Wednesday at 11:00 AM GMT+5:30
Les ventes se terminent bientôt
Inside the FDA Inspection: Managing Interviews, Requests, and FDA 483 Risk
Wednesday at 11:00 AM GMT+5:30
FDA Regulation of Social Media & Corporate Responsibility
Fri, Mar 27, 1:00 PM EDT
FDA Regulation of Social Media & Corporate Responsibility
Fri, Mar 27, 1:00 PM EDT
FDA Guidance for Use of Social Media by Regulated Industries
Friday at 1:00 PM EST
FDA Guidance for Use of Social Media by Regulated Industries
Friday at 1:00 PM EST
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FDA Inspection Readiness
Tuesday at 11:00 AM GMT+5:30
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FDA Inspection Readiness
Tuesday at 11:00 AM GMT+5:30
Human Behavior Under FDA Scrutiny
Tue, Feb 17, 11:00 AM GMT+5:30
Human Behavior Under FDA Scrutiny
Tue, Feb 17, 11:00 AM GMT+5:30
Controlling Organic Impurities in Pharma- ICH, Q3A or Q3B & FDA Compliance
Wed, Feb 11, 1:00 PM EST
Controlling Organic Impurities in Pharma- ICH, Q3A or Q3B & FDA Compliance
Wed, Feb 11, 1:00 PM EST
Les ventes se terminent bientôt
Medical Device Software Validation that Meets FDA Requirements
Thursday at 1:00 PM EST
Les ventes se terminent bientôt
Medical Device Software Validation that Meets FDA Requirements
Thursday at 1:00 PM EST
Controlling Organic Impurities in Pharma- ICH, Q3A or Q3B & FDA Compliance
Wed, Feb 11, 1:00 PM EST
Controlling Organic Impurities in Pharma- ICH, Q3A or Q3B & FDA Compliance
Wed, Feb 11, 1:00 PM EST
US FDA Labeling Requirements for Medical Devices
Tue, Feb 10, 1:00 PM EST
US FDA Labeling Requirements for Medical Devices
Tue, Feb 10, 1:00 PM EST
Designing Safer Medical Devices: ISO 62366 & FDA Human Factors Guidelines
Thu, Mar 19, 1:00 PM EDT
Designing Safer Medical Devices: ISO 62366 & FDA Human Factors Guidelines
Thu, Mar 19, 1:00 PM EDT
Risk Management for AI in Medical Devices: Insights from FDA's Lifecycle
Tue, Mar 10, 1:00 PM EDT
Risk Management for AI in Medical Devices: Insights from FDA's Lifecycle
Tue, Mar 10, 1:00 PM EDT
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Quality Management Systems and Data Integrity in FDA-Regulated Environments
Tuesday at 1:00 PM EST
Les ventes se terminent bientôt
Quality Management Systems and Data Integrity in FDA-Regulated Environments
Tuesday at 1:00 PM EST
Les ventes se terminent bientôt
FDA Recalls Masterclass: Proactive Preparation and Post-Recall Compliance
Tuesday at 12:00 PM EST
Les ventes se terminent bientôt
FDA Recalls Masterclass: Proactive Preparation and Post-Recall Compliance
Tuesday at 12:00 PM EST
Les ventes se terminent bientôt
FDA Registration, Listing & Facility Licensing
Thursday at 11:00 AM GMT+5:30
Les ventes se terminent bientôt
FDA Registration, Listing & Facility Licensing
Thursday at 11:00 AM GMT+5:30
Inspection Close-Out, Enforcement Risk, and Long-Term FDA Relationship
Wed, Feb 18, 11:00 AM GMT+5:30
Inspection Close-Out, Enforcement Risk, and Long-Term FDA Relationship
Wed, Feb 18, 11:00 AM GMT+5:30
US Regulation of Advertising and Promotion for Drugs and Biologics
Wed, Mar 18, 12:00 PM EDT
US Regulation of Advertising and Promotion for Drugs and Biologics
Wed, Mar 18, 12:00 PM EDT
US Regulation of Advertising and Promotion for Drugs and Biologics
Wed, Mar 18, 12:00 PM EDT
US Regulation of Advertising and Promotion for Drugs and Biologics
Wed, Mar 18, 12:00 PM EDT
Vient d'être ajouté
FDA Inspections After QMSR: What Replaces QSIT 2.0
Mon, Mar 23, 11:00 AM GMT+5:30
Vient d'être ajouté
FDA Inspections After QMSR: What Replaces QSIT 2.0
Mon, Mar 23, 11:00 AM GMT+5:30
Master Validation Plan for FDA cGMP Compliance – Live Online Training
Thu, Feb 19, 11:00 AM EST
Master Validation Plan for FDA cGMP Compliance – Live Online Training
Thu, Feb 19, 11:00 AM EST

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