Industry: Medical Devices

LIVE WEBINARS

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Medical Devices
By: Danielle DeLucy
Sunshine Act Reporting - Clarification for Clinical Research
22 January (Wednesday)
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Medical Devices
By: Charles H. Paul
FDA Audit Best Practices - Do's and Don'ts
28 January (Tuesday)
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Medical Devices
By: Danielle DeLucy
Batch Record Review and Product Release
03 February (Monday)
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Medical Devices
By: Rachelle D Souza
Principles & Practices for the Cybersecurity of Legacy Medical Devices by the International Medical Device Regulators Forum
12 February (Wednesday)
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RECORDED SESSION

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Medical Devices
By: Charles H. Paul
Project Management for Non-Project Managers - How to communicate project actions and progress - conducting effective project review meeti…
60 Minutes
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Medical Devices
By: Alan M Golden
Impact Assessments For Supplier Change Notices
60 Minutes
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Medical Devices
By: Ginette M. Collazo
Human Error Reduction Techniques for Floor Supervisors
90 Minutes
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Medical Devices
By: Alan M Golden
Validation Sampling Plans
60 Minutes
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Medical Devices
By: Jose Ignacio Mora
Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Con…
60 Minutes
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Medical Devices
By: Ginette M. Collazo
How to Write Procedures to Avoid Human Errors
90 Minutes
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Medical Devices
By: Shini Menon
Impact of machine learning in pre-clinical research and regulatory compliance
60 Minutes
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Medical Devices
By: Charles H. Paul
Project Management for Non-Project Managers - Scheduling your Project
90 Minutes
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Medical Devices
By: Carolyn Troiano
COTS, Cloud, and SaaS Systems and FDA Validation Compliance
90 Minutes
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Medical Devices
By: Alan M Golden
Validation Statistics for Non-Statisticians
60 Minutes
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Medical Devices
By: Alan M Golden
Design Control for Medical Devices and Combination Products
60 Minutes
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Medical Devices
By: Charles H. Paul
Risk Analysis in the Medical Device Design Process
90 Minutes
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Medical Devices
By: Danielle DeLucy
Successful Supplier Audits
60 Minutes
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Medical Devices
By: Edwin Waldbusser
Medical Device Hazard analysis following ISO 14971
60 Minutes
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Medical Devices
By: Charles H. Paul
Risk Assessment for Medical Devices
60 Minutes
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Medical Devices
By: Charles H. Paul
Project Management for Non-Project Managers
60 Minutes
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Medical Devices
By: Danielle DeLucy
Implementing a Change Control Quality System Successfully
60 Minutes
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Medical Devices
By: Ginette M. Collazo
Human Error Reduction in GMP Related Environments
60 Minutes
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Medical Devices
By: Ginette M. Collazo
Human Error Reduction in GMP Manufacturing Environments for Floor Supervisors
90 Minutes
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Medical Devices
By: Jose Ignacio Mora
Medical Device Software Per IEC 62304
60 Minutes
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Medical Devices
By: Edwin Waldbusser
Software Validation for the New FDA Inspections
60 Minutes
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Medical Devices
By: Danielle DeLucy
Proper Execution of Annual Product Reviews
60 Minutes
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Medical Devices
By: Danielle DeLucy
Developing an Effective CAPA Management and Root Cause Analysis System
60 Minutes
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Medical Devices
By: Don Hurd
Risk Management Under ISO 14971 Integrating Concepts From IEC 62304 and ANSI 62366
75 Minutes
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Medical Devices
By: Jose Ignacio Mora
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
90 Minutes
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Medical Devices
By: Pamela Joslin
Understand CERT Findings and What Your Organization Should Be Monitoring
60 Minutes
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Medical Devices
By: David R. Dills
FDAs Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
60 Minutes
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Medical Devices
By: Loren Gelber
FDA Regulations for Pharmaceutical Good Manufacturing Practice (GMP)
90 Minutes
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Medical Devices
By: Jeff Kasoff
Best practices for purchasing and supplier controls in the medical device industry
60 Minutes
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Medical Devices
By: Joy McElroy
Gaining And Re-Establishing Control Of Your Cleanroom
60 Minutes
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Medical Devices
By: Danielle DeLucy
Preparing And Investigating Oos/Oot Results In A Regulated Environment
60 Minutes
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