Category:
Author:

Medical device Training

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


Computer System Validation Professional Certification Program 3 Days
This 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
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
August 12-13 This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas Kelly Thomas
€1.295
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
June 15-16 This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas Kelly Thomas
$1,599
Production and Process Controls for Medical Devices What You Need to Know
30 June This webinar can help you prevent serious issues such as these. You’ll learn about FDA quality system regulation expectations, and how you can successfu
Susanne Manz Susanne Manz
$287
Medical Device Cybersecurity and FDA Compliance
06 July 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
Root Cause Analysis Techniques and CAPA Management
7 July This webinar will give you a systematic approach that utilizes quality tools to objectively identify factors that have resulted in or could contribute to
Kelly Thomas Kelly Thomas
$299
Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
07 July This webinar will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning and Plan(s)
John E Lincoln John E Lincoln
$199
Excel Spreadsheet Validation-Step-by-step guide to data integrity compliance in the COVID-19 Era
08 July This session will make you a better Excel user, saving you time and costs
David Nettleton David Nettleton
$249
Understanding Medical Device Design Controls What, Why, and How
On 19 July 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 Regulation of Artificial Intelligence/ Machine Learning
21 July This webinar is not a programming course but will explain the present and future regulatory requirements for AI/ML
Edwin Waldbusser Edwin Waldbusser
$265
21 CFR Part 11 (Electronic Records/Electronic Signatures) Compliance for Computer Systems Regulated
03 Aug 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
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
$299
Multiplicity: When and How to Adjust for Multiple Testing
5 Aug Speaker 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
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 Aug 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
3 Hrs Webinar on What You Need to Know: Investigating Out-of-Specification (OOS)
16 Sep This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA
Danielle DeLucy Danielle DeLucy
$399
Full Day Virtual Workshop Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Syst
21 Sep This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated
Joy L. McElroy Joy L. McElroy
$595
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
Learn the Latest FDA Compliance and Mobile Applications Live Webinar
02 Nov This topic is focused on the use of mobile applications to process data regulated by FDA. These applications may be used to collect, analyze, transfer
Carolyn Troiano Carolyn Troiano
$199
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
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
Medical Device Directive (MDD) to Medical Device Regulation (MDR) Transition Training Course Online
On Demand 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
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
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