Scheduled Training Courses

Training NameSpeakerTraining LevelTraining Options 
Complaint Handling from Intake to Closure David R. Dills Intermediate
Live, Mon, May 22, 2017
OnDemand Recording
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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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Establish and Maintain an Effective Supplier Qualification Program David R. Dills Intermediate
Live, Tue, Jun 06, 2017
OnDemand Recording
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The 510(k) Submission: Requirements, Contents, and Options Jeff Kasoff Intermediate
Live, Fri, Jun 09, 2017
OnDemand Recording
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Risk Based Medical Device Design Control Edwin Waldbusser Intermediate
Live, Thu, Jun 15, 2017
OnDemand Recording
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Efficient and Effective FDA and ISO Management Reviews Betty Lane Intermediate
Live, Thu, Jun 22, 2017
OnDemand Recording
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3 Hour Virtual Seminar : Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process Jeff Kasoff Intermediate
Live, Tue, Jun 27, 2017
OnDemand Recording
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The Use and Misuse of FMEA in Medical Device Risk Management Dev Raheja Intermediate
Live, Wed, Jun 28, 2017
OnDemand Recording
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CE Marking: Obtaining and Maintaining EU Compliance Under the Medical Device Directive Jeff Kasoff Intermediate
Live, Tue, Jul 11, 2017
OnDemand Recording
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Qualification of contract manufacturer organizations based on practical experience Edwin Waldbusser Intermediate
Live, Thu, Jul 20, 2017
OnDemand Recording
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Complaint Handling from Intake to Closure David R. Dills Intermediate
Live, Mon, May 22, 2017
OnDemand Recording
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6 hours webinar -Corrective and Preventive Action in FDA- and ISO-Regulated Industry Jeff Kasoff Intermediate
Live, Coming Soon..
OnDemand Recording
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3-hour Virtual Seminar : Complaint Handling in Compliance with FDA and ISO Regulations Jeff Kasoff Intermediate
Live, Coming Soon..
OnDemand Recording
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3-hour Virtual Seminar-Learning Design Controls through review of FDA 483 Observations Mercedes Massana Intermediate
Live, Coming Soon..
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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Process Validation Principles and Protocols Jeff Kasoff 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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