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Online Virtual Instructor-Led Medical Device Training

The same great training, from the comfort of your home or office

Virtual classes are available as open enrollment seminars or private training events. A private virtual seminar is ideal if you are looking to train 5 or more.

Most public seminars run daily from 1:00-5:00 p.m. Eastern time (ET). Certified classes that require a final exam have extra time on the last day to administer the final exam. 

See our Virtual Learning FAQs »

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Upcoming Public Virtual Instructor-Led Classes

Looking for more dates and classes? Visit Medical Device RA/QA Classes 


SOP Writing and Process Mapping for Medical Device Regulations

Learn how to develop and maintain a document management system that complies with requirements.

  • November 30 | Daily 1:00  -  5:00 p.m. ET

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EU MDR Auditor Training

Designed for experienced auditors who need to perform internal and supplier audits to the EU MDR requirements.

  • December 7 - 11 | Mon - Thurs 1:00 -  5:00 p.m.; Fri 11:30 - 5:00 p.m. ET

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QMS Training for Medical Devices: FDA QSR & ISO 13485

Understand the basic requirements of FDA's QSR and ISO 13485:2016 - "QMS 101".

  • December 7 - 11 | Daily 1:00  -  5:00 p.m. ET

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Medical Device Software Development, Verification, and Validation Trainings

Learn how to apply US and international regulatory requirements and standards for the design and validation of medical device software, including IEC 62304, IEC 80001, and ISO 13485 software requirements. 

  • December 7 - 10  | Daily 1:00 -  5:00 p.m. ET

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Process Validation Training for Medical Devices: Principles and Protocols

Take a simple process through the entire validation cycle – writing protocols, determining key operating parameters, and identifying data analysis strategies as you learn best practices for the practical application of process validation in medical device manufacturing.

  • December 7 - 11 | Daily 1:00 -  5:00 p.m. ET

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Design Control Training for Medical Devices

The process of design control - from establishing and verifying inputs to managing change. 

  • December 7 - 11 | Daily 1:00 -  5:00 p.m. ET

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Implementing the EU's New In Vitro Diagnostic Regulation Training (IVDR 2017/746)

In this class you’ll learn about the significant new requirements found in the IVDR, their impact on manufacturers, and how to plan an effective and efficient transition to the IVDR.

  • December 14 - 18 | Daily 1:00 -  5:00 p.m. ET

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Medical Device Complaint Management, Event Reporting, and Recall Management 

Understand the global requirements complaint handling and event reporting with a focus on the US, EU, the new EU MDR, and MDSAP countries.

  • December 14 - 18 | Daily 1:00 -  5:00 p.m. ET

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Implementing the New EU MDR

Learn the latest in EU MDR interpretation gleaned from our work with Notified Bodies, EU thought leaders, and device organizations making the transition.

  • December 14 - 18 | Daily 1:00  -  5:00 p.m. ET

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ISO 14971 Medical Device Risk Management Training

Learn how to apply ISO 14971:2019 risk management from a product and a process focus.

  • December 14 - 18 | Daily 1:00 -  5:00 p.m. ET

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Internal Auditing to MDSAP 

Designed for experienced auditors, this intensive class will teach you how to apply MDASP's process-based audit approach and align your current internal audit program to the MDSAP requirements. 

  • December 14 - 18 | Mon - Thurs -1:00  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. ET

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Medical Device Data Integrity and 21 CFR Part 11 Training

Make sure your organizations records meet US 21 CFR Part 11 requirements.

  • December 15 - 16 | Daily 1:00 -  5:00 p.m. ET

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Medical Device Cybersecurity Risk Management

If your company makes connected devices, you know cybersecurity is paramount. This virtual instructor-led training digs deep into standards affecting cybersecurity, regulations, CVSS and more.

  • January 5 - 8 | Daily 1:00  -  5:00 p.m. ET

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Conducting A Remote Medical Device QMS Audit

In this Exemplar Global-Certified class, we’ll teach you how to effectively complete all phases of the audit process in a remote format. 

  • January 5 - 6 | Daily 1:00  -  5:00 p.m. ET

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ISO 13485 Lead Auditor Training

In this virtual Lead Auditor training you'll learn the relevant skills and knowledge you need to audit quality management systems for medical devices (QMS). 

This class is delivered across 2 weeks (9 days in total). Each session except for the final session is 4 hours per day. Extra time is added to the final class in order to administer the final exam.   

  • January  11 - 21
    >> Week 1: Jan 11 - 15   | Daily 1:00 -  5:00 p.m. ET
    >> Week 2: Jan 18 - 21 | Mon - Wed - 1:00  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m. ET
     
  • February 1 - 11
    >> Week 1: Feb 1 - 5  | Daily 1:00 -  5:00 p.m. ET
    >> Week 2: Feb 8 - 11 | Mon - Wed - 1:00  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m. ET

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CER (Clinical Evaluation Report) Training for EU MDR Compliance

Learn all aspects of clinical evaluation from planning to postmarket clinical follow-up so your CERs can withstand Notified Body scrutiny.

  • January 11 - 15 | Daily 1:00  -  5:00 p.m. ET

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EU IVDR Auditor Training (Europe's In Vitro Diagnostic Regulation 2017/746)

For experienced auditors who need to audit perform internal or supplier audits to EU IVDR.

  • January 18 - 22 | Mon - Thurs 1:00 -  5:00 p.m.; Fri 11:30 - 5:00 p.m. ET

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Medical Device Supplier Quality Management Training

Don't let your suppliers get YOU in hot water! The course teaches best practices and tools to manage a comprehensive, risk-based, cross-functional supplier quality management system.

  • January 25 - 29 | Daily 1:00 -  5:00 p.m. ET

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ISO 14971:2019 Update Training

Designed for individuals who have a working knowledge of ISO 14971:2007 and EN ISO 14971:2012 and need to understand what's changed with ISO 14971:2019 and ISO/TR 24971:2020.

  • February 1 - 2 | Daily 1:00  -  5:00 p.m. ET

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Medical Device CAPA Training: Optimizing Your Programs

This training provides a solid understanding of all the elements of an effective CAPA program, with an emphasis on investigational tools and best practices for identifying problems, selecting solutions, and verifying effectiveness.

  • February 8 - 11 | Daily 1:00 -  5:00 p.m. ET

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ISO 13485 Internal Auditor Training 

Learn the steps to develop, implement, and audit an internal quality system that efficiently and effectively meets the requirements of ISO 13485 and ISO 9001. Exemplar Global-Certified.

  • February 8 - 12 | Mon - Thurs 1:00 -  5:00 p.m.; Fri 11:30  - 5:00 p.m. ET

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