Scheduled Training Courses

Training NameSpeakerTraining LevelTraining Options View Details
Process Validation Principles and Protocols Jeff Kasoff Intermediate
Live, Tue, Mar 28, 2017
OnDemand Recording
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Root Cause Failure Analysis Closed Loop Corrective Action Dr. Michael Abitz Intermediate
Live, Tue, Apr 04, 2017
OnDemand Recording
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Learning Design Controls through review of FDA 483 Observations Mercedes Massana Intermediate
Live, Wed, Apr 12, 2017
OnDemand Recording
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Risk-based Supplier Control: How to Meet FDA and your ISO 13485 Notified Body's Expectations and Reduce your Own Risk Betty Lane Intermediate
Live, Thu, Apr 13, 2017
OnDemand Recording
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Corrective and Preventive Action in FDA- and ISO-Regulated Industry Jeff Kasoff Intermediate
Live, Tue, Apr 18, 2017
OnDemand Recording
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Complaint Handling in Compliance with FDA and ISO Regulations Jeff Kasoff Intermediate
Live, Mon, Apr 24, 2017
OnDemand Recording
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Using an IQ / OQ / PQ Approach to Validating Medical Device Software Mercedes Massana Intermediate
Live, Wed, May 03, 2017
OnDemand Recording
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Software Validation & Testing Dev Raheja Intermediate
Live, Tue, May 09, 2017
OnDemand Recording
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Complaint Handling from Intake to Closure David R. Dills Intermediate
Live, Tue, May 16, 2017
OnDemand Recording
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How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare Jeff Kasoff --
Live, Wed, May 17, 2017
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Designing Medical Device Alarms to Mitigate New FDA Concerns Dev Raheja Intermediate
Live, Tue, May 23, 2017
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Best Practices for FDA and ISO 13485 Corrective Actions Betty Lane Intermediate
Live, Thu, May 25, 2017
OnDemand Recording
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Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration Jose Mora Intermediate
Live, Coming Soon..
OnDemand Recording
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21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration Jose Mora Intermediate
Live, Coming Soon..
OnDemand Recording
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ISO 14971 Risk Management and Risk Management Process Susanne Manz Intermediate
Live, Coming Soon..
OnDemand Recording
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6-hr Virtual Seminar: Medical Device Regulations and Evolving Requirements: Post Market Surveillance, Complaint Handling, eMDR, Recalls , UDI Regulations and Emerging Signals Susanne Manz Advanced
Live, Coming Soon..
OnDemand Recording
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FDA 21 CFR Part 11 for Techies and Management Alfonso Fuller Intermediate
Live, Coming Soon..
OnDemand Recording
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Verification and Validation Planning John E. Lincoln Intermediate
Live, Coming Soon..
OnDemand Recording
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Understanding Failure Mode Effects Analysis William A. Levinson Intermediate
Live, Coming Soon..
OnDemand Recording
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3-hr Virtual Seminar: Design Controls for Medical Devices Susanne Manz Intermediate
Live, Coming Soon..
OnDemand Recording
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Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration Jose Mora Intermediate
Live, Coming Soon..
OnDemand Recording
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Qualification of Facilities and Equipment Igor Gorsky Advanced
Live, Coming Soon..
OnDemand Recording
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3-hr Virtual Seminar: Understanding FDA Expectations for Root Cause Analysis Susanne Manz Intermediate
Live, Coming Soon..
OnDemand Recording
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2-hr Virtual Seminar: Preparing for and Managing EU Notified Bodies Audits as a Result of EU Commission Recommendation 2013/473/EU Vanessa Lopez Intermediate
Live, Coming Soon..
OnDemand Recording
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Purchasing Controls - Enabling You to Provide Safe and Effective Products Susanne Manz Intermediate
Live, Coming Soon..
OnDemand Recording
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