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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


Medical Device Directive (MDD) to Medical Device Regulation (MDR) Transition Training Course Online
06-28 Apr Virtual Training Online on EU-MDR to align your company with the new requirements of the Medical Device Regulation (EU-MDR) by UK top Industry Expert
Frank Stein Frank Stein
€1.695
Medical Device Directive (MDD) to Medical Device Regulation (MDR) Transition Training Course Online
06-28 Apr Virtual Training Online on EU-MDR to align your company with the new requirements of the Medical Device Regulation (EU-MDR) by UK top Industry Expert
Frank Stein Frank Stein
$1,495
FDA’s Plan for Modernizing the 510(k) Pathway
20 April 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
Vaccine Patents in the Current Pandemic Climate Live Webinar
21 Apr This presentation will discuss not only the global patenting issues facing vaccines but will also look at some of the challenges facing vaccine patenting
Joanna Brougher Joanna Brougher
$199
Hypothesis Testing, p-values, and Inference: When Thinking Like a Statistician Makes Sense
22 April 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
$1,025
The Veterinary Drug Approval Process and FDA Regulatory Oversight
April 22-23 -This two-day seminar will provide attendees with an understanding of FDA’s veterinary drug approval process, obtaining federal government approval.
Karl M. Nobert Karl M. Nobert
$1,899
Knock, knock, who’s there? Are you ready for an FDA inspection in the COVID-19 Era and Beyond?
27 April This webinar will help you manage inspections efficiently and effectively. You’ll learn about the FDA’s inspectional approach, focus areas and prepare
Susanne Manz Susanne Manz
$389
Computer System Validation Professional Certification Program 3 Days
April 27-29
Carolyn Troiano Carolyn Troiano
$1,495
FDA Computer System Validation ( CSV) Training 3 Days Virtual Seminar
On April 27-29 this Course will explain 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
$1,495
Understanding Medical Device Design Controls What, Why, and How
On 06 May this FDA Design Control course online is US-focused. The participants will gain a fundamental understanding of how medical devices are regulated.
Alan Golden Alan Golden
$599
FDA Recalls - Before You Start, and After You Finish
On 11 - 12 May, 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
$1,599
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
On 18-19-May, 2021 this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Kelly Thomas Kelly Thomas
$1,599
Excel Spreadsheet Validation-Step-by-step guide to data integrity compliance in the COVID-19 Era
19 May This session will make you a better Excel user, saving you time and costs
David Nettleton David Nettleton
$249
21 CFR Part 11, SaaS/Cloud, EU GDPR - What Regulatory, Quality & Compliance Professionals Need to Know
01 June 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
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
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
Learn the Latest FDA Compliance and Mobile Applications Live Webinar
MP3 Download Duration 90 Minutes
Carolyn Troiano Carolyn Troiano
$199
Continuing to Audit during a Global Pandemic – How to Optimize Effectiveness and Minimize Risk
MP3 Download Duration 60 Minutes
Susanne Manz Susanne Manz
$249
Medical Device Cybersecurity and FDA Compliance
MP3 Download Duration 90 Minutes
Carolyn Troiano Carolyn Troiano
$229
DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR Requirements
MP3 Download / Online On Demand-Duration 180 Minutes
John E Lincoln John E Lincoln
$399
Learn the latest Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance Webinar
MP3 Download Duration 90 Minutes
Carolyn Troiano Carolyn Troiano
$199
3 Hrs Webinar on What You Need to Know: Investigating Out-of-Specification (OOS)
MP3 Download Duration 180 Minutes
Danielle DeLucy Danielle DeLucy
$399
Understanding the Design Verification and Validation Requirements for Medical Devices
MP3 Download Duration 60 Minutes
Meena Chettiar Meena Chettiar
$199
FDA Regulation of Artificial Intelligence/ Machine Learning
MP3 Download Duration 60 Minutes
Edwin Waldbusser Edwin Waldbusser
$199
Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
MP3 Download Duration 60 Minutes
John E Lincoln John E Lincoln
$399
21 CFR Part 11 (Electronic Records/Electronic Signatures) Compliance for Computer Systems Regulated
MP3 Download You will learn how to comply with FDA's 21 CFR Part 11 guidance, which addresses the use of electronic records and electronic signatures
Carolyn Troiano Carolyn Troiano
$299
How to write SOP's that Avoid Human Error
MP3 Download Duration 90 Minutes
Ginette Collazo Ginette Collazo
$199
Why people make mistakes. Understanding Human error
MP3 Download Duration 90 Minutes
Ginette Collazo Ginette Collazo
$199
Quality Control Laboratory Compliance - cGMPs and GLPs
MP3 Download Duration 2 Day
Kelly Thomas Kelly Thomas
$1,895
FDA Warnings - common trends and observations and how to prepare for FDA inspection
MP3 Download Duration 90 Minutes
Eleonora Babayants Eleonora Babayants
$199
Webinar FDA’s Regulatory Management of Your Cybersecurity Threats
MP3 Download -Duration 60 Minutes
Casper (Cap) Uldriks Casper (Cap) Uldriks
$199
Masterclass: 4 Keys to Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations
MP3 Download Duration 120 Minutes
John G. Lanese John G. Lanese
$499
Learn the latest webinar Software Validation Utilizing Principles of Lean Documents and Lean Configuration
24-Feb,2021 at 01:00 PM ET | 10:00 AM PT | 12:00 PM CT Duration 90 Minutes
Jose Mora Jose Mora
$199