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Événements fda En Ligne

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
FDA Inspection Essentials
Thu, May 22, 10:00 AM GMT+5:30
FDA Inspection Essentials
Thu, May 22, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On U.S. FDA And EU Medical Device
Wed, Jun 4, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On U.S. FDA And EU Medical Device
Wed, Jun 4, 10:00 AM GMT+5:30
A RISK BASED APPROACH TO IT INFRASTRUCTURE QUALIFICATION & COMPLIANCE
Tue, Jun 10, 10:00 AM GMT+5:30
A RISK BASED APPROACH TO IT INFRASTRUCTURE QUALIFICATION & COMPLIANCE
Tue, Jun 10, 10:00 AM GMT+5:30
Cyber Security Planning for Medical Devices
Fri, Jul 11, 10:00 AM GMT+5:30
Cyber Security Planning for Medical Devices
Fri, Jul 11, 10:00 AM GMT+5:30
Supplier Management with the new EU MDR 745/2017
Wed, May 28, 10:00 AM GMT+5:30
Supplier Management with the new EU MDR 745/2017
Wed, May 28, 10:00 AM GMT+5:30
Audit Like the FDA - Effective Internal Audit Program
Fri, May 23, 10:00 AM GMT+5:30
Audit Like the FDA - Effective Internal Audit Program
Fri, May 23, 10:00 AM GMT+5:30
Preventive Maintenance And Calibrations - Regulatory Expectations
Wed, Jun 4, 10:00 AM GMT+5:30
Preventive Maintenance And Calibrations - Regulatory Expectations
Wed, Jun 4, 10:00 AM GMT+5:30
Validation Of Artificial Intelligence (AI), Machine Learning (ML)
Fri, May 30, 10:00 AM GMT+5:30
Validation Of Artificial Intelligence (AI), Machine Learning (ML)
Fri, May 30, 10:00 AM GMT+5:30
The US FDA QMSR Transition - 21 CFR 820 And ISO 13485
Wed, Jun 4, 10:00 AM GMT+5:30
The US FDA QMSR Transition - 21 CFR 820 And ISO 13485
Wed, Jun 4, 10:00 AM GMT+5:30
Quality Control Laboratory Compliance - cGMP and GLP Training
Tue, May 20, 10:00 AM GMT+5:30
Quality Control Laboratory Compliance - cGMP and GLP Training
Tue, May 20, 10:00 AM GMT+5:30
Annual GMP Master Class 2024
Tue, May 20, 10:00 AM GMT+5:30
Annual GMP Master Class 2024
Tue, May 20, 10:00 AM GMT+5:30
Clinical Trials for The Intended Use of Software as a Medical Device
Sat, Jul 12, 10:00 AM GMT+5:30
Clinical Trials for The Intended Use of Software as a Medical Device
Sat, Jul 12, 10:00 AM GMT+5:30
EU Medical Devices Regulation – CE Mark Expiration
Wed, Jul 16, 10:00 AM GMT+5:30
EU Medical Devices Regulation – CE Mark Expiration
Wed, Jul 16, 10:00 AM GMT+5:30
A TO Z OF Analytical Method Validation, Verification and Transfer
Tue, May 20, 10:00 AM GMT+5:30
A TO Z OF Analytical Method Validation, Verification and Transfer
Tue, May 20, 10:00 AM GMT+5:30
3-HOUR VIRTUAL SEMINAR ON 510(K)'S, PMA'S, IDE'S AND DENOVO'S
Sat, Jun 21, 10:00 AM GMT+5:30
3-HOUR VIRTUAL SEMINAR ON 510(K)'S, PMA'S, IDE'S AND DENOVO'S
Sat, Jun 21, 10:00 AM GMT+5:30
Data Integrity by Design and Pharma 4.0: Next-Gen Techniques
Wed, May 21, 10:00 AM GMT+5:30
Data Integrity by Design and Pharma 4.0: Next-Gen Techniques
Wed, May 21, 10:00 AM GMT+5:30
EU's New Regulation 536/2014 On Clinical Trials
Thu, Jun 5, 10:00 AM GMT+5:30
EU's New Regulation 536/2014 On Clinical Trials
Thu, Jun 5, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On Digital Validation Demystified
Thu, May 29, 10:00 AM GMT+5:30
3-Hour Virtual Seminar On Digital Validation Demystified
Thu, May 29, 10:00 AM GMT+5:30

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