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Industry: Medical Devices

LiveWebinars

[ No Any Live Webinar Found For Medical Devices Industry! ]

Recorded Session

Impact Assessments For Supplier Change Notices
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By: Alan M Golden | Recorded Session

Duration: 60 Minutes

Validation Sampling Plans
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By: Alan M Golden | Recorded Session

Duration: 60 Minutes

Project Management for Non-Project Managers - Scheduling your Project
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By: Charles H. Paul | Recorded Session

Duration: 90 Minutes

Project Management for Non-Project Managers - How to communicate project actions and progress - conducting effective project review meetings
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By: Charles H. Paul | Recorded Session

Duration: 60 Minutes

Batch Record Review and Product Release
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

FDA Audit Best Practices - Do's and Don'ts
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By: Charles H. Paul | Recorded Session

Duration: 60 Minutes

Sunshine Act Reporting - Clarification for Clinical Research
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Human Error Reduction Techniques for Floor Supervisors
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By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration
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By: Jose Ignacio Mora | Recorded Session

Duration: 60 Minutes

How to Write Procedures to Avoid Human Errors
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By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Impact of machine learning in pre-clinical research and regulatory compliance
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By: Shini Menon | Recorded Session

Duration: 60 Minutes

COTS, Cloud, and SaaS Systems and FDA Validation Compliance
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By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

Validation Statistics for Non-Statisticians
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By: Alan M Golden | Recorded Session

Duration: 60 Minutes

Design Control for Medical Devices and Combination Products
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By: Alan M Golden | Recorded Session

Duration: 60 Minutes

Risk Analysis in the Medical Device Design Process
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By: Charles H. Paul | Recorded Session

Duration: 90 Minutes

Successful Supplier Audits
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Medical Device Hazard analysis following ISO 14971
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By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

Risk Assessment for Medical Devices
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By: Charles H. Paul | Recorded Session

Duration: 60 Minutes

Project Management for Non-Project Managers
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By: Charles H. Paul | Recorded Session

Duration: 60 Minutes

Implementing a Change Control Quality System Successfully
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Human Error Reduction in GMP Related Environments
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By: Ginette M. Collazo | Recorded Session

Duration: 60 Minutes

Human Error Reduction in GMP Manufacturing Environments for Floor Supervisors
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By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Medical Device Software Per IEC 62304
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By: Jose Ignacio Mora | Recorded Session

Duration: 60 Minutes

Software Validation for the New FDA Inspections
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By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

Proper Execution of Annual Product Reviews
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Developing an Effective CAPA Management and Root Cause Analysis System
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Risk Management Under ISO 14971 Integrating Concepts From IEC 62304 and ANSI 62366
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By: Don Hurd | Recorded Session

Duration: 75 Minutes

Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
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By: Jose Ignacio Mora | Recorded Session

Duration: 90 Minutes

Understand CERT Findings and What Your Organization Should Be Monitoring
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By: Pamela Joslin | Recorded Session

Duration: 60 Minutes

FDAs Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
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By: David R. Dills | Recorded Session

Duration: 60 Minutes

FDA Regulations for Pharmaceutical Good Manufacturing Practice (GMP)
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By: Loren Gelber | Recorded Session

Duration: 90 Minutes

Best practices for purchasing and supplier controls in the medical device industry
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By: Jeff Kasoff | Recorded Session

Duration: 60 Minutes

Preparing And Investigating Oos/Oot Results In A Regulated Environment
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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Gaining And Re-Establishing Control Of Your Cleanroom
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By: Joy McElroy | Recorded Session

Duration: 60 Minutes