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Événements fda En Ligne

FDA Labeling and UDI Essentials for Medical Products
Wed, May 28, 10:00 AM GMT+5:30
FDA Labeling and UDI Essentials for Medical Products
Wed, May 28, 10:00 AM GMT+5:30
Trimming Back the Burden of FDA’s Software Regulation
Wed, Jul 16, 10:00 AM GMT+5:30
Trimming Back the Burden of FDA’s Software Regulation
Wed, Jul 16, 10:00 AM GMT+5:30
FDA Guidance: Design Considerations for Pivotal Clinical Investigations
Fri, Jul 11, 10:00 AM GMT+5:30
FDA Guidance: Design Considerations for Pivotal Clinical Investigations
Fri, Jul 11, 10:00 AM GMT+5:30
Handling OOS Test Results and Robust Investigations
Wed, Dec 31, 10:00 AM GMT+5:30
Handling OOS Test Results and Robust Investigations
Wed, Dec 31, 10:00 AM GMT+5:30
Implementing Quality by Design for Enhanced Product Quality and Patient
Mon, Mar 9, 1:00 PM EDT
Implementing Quality by Design for Enhanced Product Quality and Patient
Mon, Mar 9, 1:00 PM EDT
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
Training Requirements under FDA’s Quality System Regulation
Sat, Jul 12, 10:00 AM GMT+5:30
Training Requirements under FDA’s Quality System Regulation
Sat, Jul 12, 10:00 AM GMT+5:30
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
6-Hour Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Thu, Jan 15, 10:00 AM EST
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
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
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
Excellence in Documentation Practices and Regulatory Compliance (FDA & EMA)
Thu, Jan 8, 1:00 PM EST
Excellence in Documentation Practices and Regulatory Compliance (FDA & EMA)
Thu, Jan 8, 1:00 PM EST
Investigating Out-of-Specification (OOS) Test Results in the Laboratory
Fri, Jan 9, 1:00 PM EST
Investigating Out-of-Specification (OOS) Test Results in the Laboratory
Fri, Jan 9, 1:00 PM EST
Achieving Compliance Through Effective Documentation Practices (FDA & EMA)
Thu, Jan 8, 1:00 PM EST
Achieving Compliance Through Effective Documentation Practices (FDA & EMA)
Thu, Jan 8, 1:00 PM EST
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

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