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Événements fda En Ligne

The FDA Inspection From SOP To 483
Thu, Jun 5, 10:00 AM GMT+5:30
The FDA Inspection From SOP To 483
Thu, Jun 5, 10:00 AM GMT+5:30
Step-by-Step approach for Setting up FDA Audit Ready Quality Management
Tue, Jul 8, 10:00 AM GMT+5:30
Step-by-Step approach for Setting up FDA Audit Ready Quality Management
Tue, Jul 8, 10:00 AM GMT+5:30
FDA REGULATION OF ARTIFICIAL INTELLIGENCE / MACHINE LEARNING
Tue, Jul 8, 10:00 AM GMT+5:30
FDA REGULATION OF ARTIFICIAL INTELLIGENCE / MACHINE LEARNING
Tue, Jul 8, 10:00 AM GMT+5:30
FDA Warning Letter - Consent Decree Software Validation
Wed, May 28, 10:00 AM GMT+5:30
FDA Warning Letter - Consent Decree Software Validation
Wed, May 28, 10:00 AM GMT+5:30
Ovarian Cancer Clinical Trials and Novel Therapeutics
Tue, Feb 17, 7:00 PM PST
Ovarian Cancer Clinical Trials and Novel Therapeutics
Tue, Feb 17, 7:00 PM PST
Avoid Warning Letters in View of the U.S. FDA's Stated Goal
Tue, May 27, 10:00 AM GMT+5:30
Avoid Warning Letters in View of the U.S. FDA's Stated Goal
Tue, May 27, 10:00 AM GMT+5:30
FDA’S RECENT REGULATION ON THE USE OF SOCIAL MEDIA
Tue, Jun 10, 10:00 AM GMT+5:30
FDA’S RECENT REGULATION ON THE USE OF SOCIAL MEDIA
Tue, Jun 10, 10:00 AM GMT+5:30
Managing the FDA form “483”: Inspection Observations
Sat, Jul 12, 10:00 AM GMT+5:30
Managing the FDA form “483”: Inspection Observations
Sat, Jul 12, 10:00 AM GMT+5:30
Physician Medical Weight Loss Training - LiveStream/Online Training
Sun, Jan 25, 10:00 AM EST + 4 en plus
Physician Medical Weight Loss Training - LiveStream/Online Training
Sun, Jan 25, 10:00 AM EST + 4 en plus
How FDA trains its Investigators to Review CAPA and How should you prepare
Sat, Jun 21, 10:00 AM GMT+5:30
How FDA trains its Investigators to Review CAPA and How should you prepare
Sat, Jun 21, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On US FDA Cybersecurity Requirements
Fri, Jun 6, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On US FDA Cybersecurity Requirements
Fri, Jun 6, 10:00 AM GMT+5:30
The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Me
Wed, May 21, 10:00 AM GMT+5:30
The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Me
Wed, May 21, 10:00 AM GMT+5:30
Master The Vendor Auditing Of Your Computer Systems Regulated By FDA
Thu, May 29, 10:00 AM GMT+5:30
Master The Vendor Auditing Of Your Computer Systems Regulated By FDA
Thu, May 29, 10:00 AM GMT+5:30
Avoid Reporting Cybersecurity Updates and Patches to the FDA
Sat, Jul 12, 10:00 AM GMT+5:30
Avoid Reporting Cybersecurity Updates and Patches to the FDA
Sat, Jul 12, 10:00 AM GMT+5:30
Validation 101
Fri, Nov 6, 12:00 PM EST
Validation 101
Fri, Nov 6, 12:00 PM EST
Medical Device Cybersecurity Following Latest FDA Guidance
Sat, Jun 7, 10:00 AM GMT+5:30
Medical Device Cybersecurity Following Latest FDA Guidance
Sat, Jun 7, 10:00 AM GMT+5:30
EQUIPMENT QUALIFICATION AND PROCESS VALIDATION
Tue, Jun 10, 10:00 AM GMT+5:30
EQUIPMENT QUALIFICATION AND PROCESS VALIDATION
Tue, Jun 10, 10:00 AM GMT+5:30
Establishing FDA-Compliant Product Stability Testing Program
Thu, Jun 5, 10:00 AM GMT+5:30
Establishing FDA-Compliant Product Stability Testing Program
Thu, Jun 5, 10:00 AM GMT+5:30
Production And Process Controls For Medical Devices
Thu, Jun 5, 10:00 AM GMT+5:30
Production And Process Controls For Medical Devices
Thu, Jun 5, 10:00 AM GMT+5:30
Computer System Validation and Data Integrity for Clinical Trials
Thu, May 22, 10:00 AM GMT+5:30
Computer System Validation and Data Integrity for Clinical Trials
Thu, May 22, 10:00 AM GMT+5:30

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