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Industry: Medical Devices

LiveWebinars

CAPA/Root Cause Analysis: Achieving Compliance with Proper CAPA Systems

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By: Danielle DeLucy | March 30, 2023

Duration: 90 Minutes | Time: 10:00 AM PDT | 01:00 PM EDT

Risk Assessment for Medical Devices

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By: Charles H. Paul | April 3, 2023

Duration: 60 Minutes | Time: 12:00 PM PDT | 03:00 PM EDT

Recorded Session

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

Best practices for purchasing and supplier controls in the medical device industry

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By: Jeff Kasoff | 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

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

Understand CERT Findings and What Your Organization Should Be Monitoring

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By: Pamela Joslin | Recorded Session

Duration: 60 Minutes

Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration

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By: Jose Mora | Recorded Session

Duration: 90 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

Developing an Effective CAPA Management and Root Cause Analysis System

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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Proper Execution of Annual Product Reviews

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By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Software Validation for the New FDA Inspections

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By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

Medical Device Software Per IEC 62304

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By: Jose Mora | Recorded Session

Duration: 60 Minutes

How to Conduct Annual Product Reviews to Achieve GMP Compliance

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By: Danielle DeLucy | Recorded Session

Duration: 75 Minutes

Human Error Reduction in GMP Manufacturing Environments for Floor Supervisors

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By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Human Error Reduction in GMP Related Environments

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By: Ginette M. Collazo | 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

Impact Assessments For Supplier Change Notices

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By: Alan M Golden | 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

Project Management for Non-Project Managers

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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

Risk Analysis in the Medical Device Design Process

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By: Charles H. Paul | Recorded Session

Duration: 90 Minutes