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Medical device Training

Online medical device trainings, medical devices regulatory compliance trainings, webinars on FDA medical devices regulations and more from World Compliance Seminars


SaaS/Cloud Risk-Based Validation With Time-Saving Templates
03 Aug This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted
David Nettleton David Nettleton
$249
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
04 Aug This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities
Kelly Thomas Kelly Thomas
$499
Purchasing Controls, Receiving Inspection, and Supplier Audit – what to do during a global pandemic
5 Aug 2021 This webinar will provide insights into how to use remote auditing techniques to minimize the risk and maximize the benefits of conducting audits
Susanne Manz Susanne Manz
$199
Multiplicity: When and How to Adjust for Multiple Testing
5 August 2021 this webinar will explain the differences between family wise error rate (FWER) and false discovery rate (FDR).
Elaine Eisenbeisz Elaine Eisenbeisz
$249
Quality by Design for Medical Devices Live Webinar
12 Aug This webinar can help you create a design control process that is a competitive strength for your company.
Susanne Manz Susanne Manz
$699
FDA Recalls - Before You Start, and After You Finish
On 12 - 13 Aug, 2021 this seminar will help you to Understand FDA's recall authority and policy , Learn how to manage recalls under FDA oversight.
Kelly Thomas Kelly Thomas
$1,295
Computer System Validation Professional Certification Program 3 Days
August 18-20 3 day CSV course will teach you how to comply with key FDA and international CSV regulations and guidance, such as 21 CFR Part 11 and Annex 11.
Carolyn Troiano Carolyn Troiano
$1,295
Audits in the World of COVID-19 and Beyond: Are You Ready for Remote Audits?
19 August 2021 The presentation will provide an insight and guidance to managers with QA departments to implement a Remote Auditing program
Michael Ramcharan Michael Ramcharan
$229
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
On August 19-20, 2021 this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Rita Hoffman Rita Hoffman
$1,599
Hypothesis Testing, p-values, and Inference: When Thinking Like a Statistician Makes Sense
24 August 2021 You will learn the why and how of the scientific method, and how to view the world with a statistician’s eyes
Elaine Eisenbeisz Elaine Eisenbeisz
$499
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
On 24 August 2021 this webinar will cover all the items listed above, and more. If you want to improve your CAPA system, you cannot afford to miss this.
Jeff Kasoff Jeff Kasoff
$199
Post Market Surveillance - Complaint Handling and Medical Device Reporting
16 Sep This webinar will cover the basics of complaint management and medical device reporting
Susanne Manz Susanne Manz
$229
Tips for setting up a Quality System to withstand FDA Audits for Medical Device and Pharmaceutical Companies
05 Oct This webinar will provide a step by step approach and valuable tips for setting up a Quality System to withstand FDA Audits
Meena Chettiar Meena Chettiar
$199
Calculations for Process and Product Capability
21 Oct This Webinar will focus on providing the information needed for attendees to know the appropriate measures and formulas
Elaine Eisenbeisz Elaine Eisenbeisz
$249
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
On 21-23-Oct, 2021 this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Rita Hoffman Rita Hoffman
€1.295
Purchasing Controls and Receiving Acceptance for Medical Devices
02 Dec This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products
Susanne Manz Susanne Manz
$229
Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
MP3 Download This Webinar will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning.
John E Lincoln John E Lincoln
$199
How FDA trains its investigators to review CAPA and what should you do to prepare
MP3 Download This webinar will discuss all the documents used by FDA to train their inspectors to review your CAPA system, some of which you may not be familiar
Jeff Kasoff Jeff Kasoff
$199
Medical Device Cybersecurity and FDA Compliance
MP3 Download This webinar will focus on cybersecurity of medical devices, a key concern for those who develop, manufacture, test, and distribute these products
Carolyn Troiano Carolyn Troiano
$695
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
MP3 Download Learn the basic overview of the original medical device Quality Management System
John E Lincoln John E Lincoln
$229
Excel Spreadsheet Validation-Step-by-step guide to data integrity compliance in the COVID-19 Era
MP3 Download This session will make you a better Excel user, saving you time and costs
David Nettleton David Nettleton
$599
The FDA Inspection: Best Practices for Preparation, Behavior, and Response
MP3 Download This course provides medical device/pharmaceutical professionals with the information they need to prepare for and manage any type of FDA
Jeff Kasoff Jeff Kasoff
$179
Risk-Based Approach to Part 11 Compliance and Policies and Procedures to Support GxPs
MP3 Download This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle
Carolyn Troiano Carolyn Troiano
$392
FDA Regulation of Artificial Intelligence/ Machine Learning
MP3 Download This webinar is not a programming course but will explain the present and future regulatory requirements for AI/ML
Edwin Waldbusser Edwin Waldbusser
$265
How to write SOP's that Avoid Human Error
MP3 Download This Webinar will discuss the primary cause of quality and production losses in many industries
Ginette Collazo Ginette Collazo
$199
Production and Process Controls for Medical Devices What You Need to Know
MP3 Download This webinar can help you prevent serious issues such as these. You’ll learn about FDA quality system regulation expectations, and how you can
Susanne Manz Susanne Manz
$287
Identifying Sources of Process Unreliability Within Your Organization: You May be Surprised.
MP3 Download In this Webinar you will learn how to use Reality-Charting, The Model for Improvement, and Process Reliability Modeling
David W. Husman David W. Husman
$209
Dealing with CAPA- Corrective and Preventive Actions in FDA Regulated Industries
MP3 Download New Root Cause Analysis Techniques and CAPA Management live webinar is for those in Operations, Facilities , Engineering and QA/QC
Meena Chettiar Meena Chettiar
$179
Compliant Management Controls Under 21 CFR 820 and ISO 13485
MP3 Download Best QSR and ISO 13485 requirements webinar for management controls, Organizational structure and Establishment of an internal audit program.
Jeff Kasoff Jeff Kasoff
$179
Vaccine Patents in the Current Pandemic Climate Live Webinar
MP3 Download This presentation will discuss not only the global patenting issues facing vaccines but will also look at some of the challenges facing vaccine
Joanna Brougher Joanna Brougher
$199
FDA’s Plan for Modernizing the 510(k) Pathway
MP3 Download This FDA Training online will explain Basic of US FDA’s Expectations for the 510(k), The Medical Device Safety Action Plan and 510(k)
John E Lincoln John E Lincoln
$179
Supervising a Human Error Free Environment: You can do a Lot More than you Think
MP3 Download How can we prevent human error? This 90 -minutes online course will discuss why supervision is so important in reducing and preventing human error
Ginette Collazo Ginette Collazo
$179
Non-conforming Materials in a Medical Device Company – dealing with in-house to field issues
MP3 Download Join industry expert Susanne Manz to learn online the essentials of dealing with non-conforming material and performing effective failure
Susanne Manz Susanne Manz
$399
Are you ready for your next regulatory inspection? On site or virtual in 2021
MP3 Download This webinar is a practical, hands-on course designed to provide FDA industry with information and tools required to prepare for and manage an FDA
Alan Golden Alan Golden
$399
Continuing to Audit during a Global Pandemic – How to Optimize Effectiveness and Minimize Risk
MP3 Download Duration 60 Minutes
Susanne Manz Susanne Manz
$249
Knock, knock, who’s there? Are you ready for an FDA inspection in the COVID-19 Era and Beyond?
MP3 Download This webinar will help you manage inspections efficiently and effectively. You’ll learn about the FDA’s inspectional approach, focus areas
Susanne Manz Susanne Manz
$389