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Understanding Combination Products: Navigating the Rules and Regulations
Charles H. Paul
LIVE : April 30 , 2024 01:00 PM EDT
Life Sciences > Medical Devices
Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant...
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European Union Device Regulation (EU MDR)
Edwin Waldbusser
LIVE : May 01 , 2024 01:00 PM EDT
Life Sciences > Medical Devices
Ed retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. He was involved in the development ...
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Risk Based Design Control
Edwin Waldbusser
LIVE : May 15 , 2024 01:00 PM EDT
Life Sciences > Medical Devices
Ed retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. He was involved in the development ...
Showing 101-110 of 132 items.
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Reliability Engineering Fundamentals for Medical Devices
Dev Raheja
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies ev...
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UDI Program Implementation
Dev Raheja
Recorded Duration : 75 Minutes
Life Sciences > Medical Devices
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies ev...
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ISO 13485: 2016 - Understanding and Implementing The International Medical Device Quality Standard
Meena Chettiar
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices

Ms. Chettiar received her M.S. in Regulatory Affairs for Medical Devices in Minnesota, USA, and M.A.SC in Chemical Engineering from University ...

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Medical Device Complaints Handling Management-- One Of top Citations During FDA Inspection
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
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Medical Device Registration and Approval Process for The Pacific Rim (Including China, Singapore, Ta...
David R. Dills
Recorded Duration : 60 Minutes
Life Sciences > Medical Devices
David R. Dills, is an independent Global Regulatory Affairs & Compliance Consultant and has an accomplished record with more than 27 years of experience in regulatory affa...
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Quality Metrics and Risk Based Inspections: Quality Metrics Guidance for Industry & Safety and Innov...
Angela K. Dunston
Recorded Duration : 60 Minutes
Life Sciences > Medical Devices
Angela K. Dunston has over 20 years of experience in manufacturing and laboratory quality and compliance in the pharmaceutical, biotechnology, and medical device (diagnostics)...
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Raw Materials Risk Management In GMP Facilities: Avoiding GMP Non-Compliance Due to Raw Material Iss...
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
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Reprocessing Reusable Medical Devices Cleaning & Labeling Requirements
John Chapman
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
John Chapman, BS, MBA, RAC has over 35 years medical device regulatory experience and over 15 years experience with the European Union’s medical device directive, 93/42/EEC....
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How the FDA are Trained for Medical Device Inspections
Angela Bazigos
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
Angela Bazigos, is the CEO of Touchstone Technologies, Inc. She has 40 years of experience working in hospitals and Pharma industry. Her background includes companies like Roc...
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Essentials of Medical Device Reporting and Complaint Handling
Susanne Manz
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background ...
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