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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.

Public seminars typically run  daily from 1:30-5:00 p.m. EST (3.5 hours each day). Certified classes that require a final exam are extended by 2 hours on the last day to administer the final exam. 

See our Virtual Learning FAQs »

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Upcoming Public Virtual Instructor-Led Classes

Visit Medical Device RA/QA Classes to see a complete list of courses.

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.  

  • July 1- 2 | 1:30  -  5:00 p.m. (EST)
  • July 29 - 30 | 1:30  -  5:00 p.m. (EST)

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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.   

  • July 6 - 10 | Daily 1:30  -  5:00 p.m. (EST)

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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 3.5 hours per day. The final class is extended by 2 hours in order to administer the final exam.   

  • July 6 - July 16 
    >> Week 1: July 6 - 10  | Daily 1:30 -  5:00 p.m. (EST)
    >> Week 2: July 13 - 16  | Mon - Wed -1:30  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m. (EST)
     
  • July 20 - July 30
    >> Week 1: July 20 - 24   | Daily 1:30 -  5:00 p.m. (EST)
    >> Week 2: July 27 - 30  | Mon - Wed -1:30  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m. (EST)

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EU IVDD to IVDR Transition Training

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.

  • July 13 - 17 | Daily 1:30 -  5:00 p.m. (EST)

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Updated! ISO 14971:2019 Medical Device Risk Management Training

In this workshop-based course you will learn how to apply ISO 14971 risk management from a product focus and a process focus.

  • July 20 - 24 | Daily 1:30  -  5:00 p.m. (EST)

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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".

  • July 20 - 24 | Daily 1:30  -  5:00 p.m. (EST)

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EU MDR Transition Training

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

  • July 20 - 24 | Daily 1:30 -  5:00 p.m. (EST)

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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.

  • July 27 - 31 | Mon - Thurs 1:30 -  5:00 p.m.; Fri 11:30 - 5:00 p.m. (EST)

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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.

  • August 10 - 13 | Daily 1:30  -  5:00 p.m (EST)

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Medical Device Software Development, Verification, and Validation Training

Learn how to apply US and international regulatory requirements and standards for the design and validation of medical device software.

  • August 17 - 21 | Daily 1:30 -  5:00 p.m. (EST)

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Medical Device Complaint Management and Vigilance Training 

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

  • August 10 - 14 | Daily 1:30 -  5:00 p.m. (EST)

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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.

  • August 3 - 7 | Mon - Thurs 1:30 -  5:00 p.m.; Fri 11:30  - 5:00 p.m. (EST)

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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. 

  • August 3  - 7 | Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. (EST)

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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.

  • August 31 - Sept 4 | Daily 1:30 -  5:00 p.m. (EST)

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Medical Device Root Cause Analysis Training 

How to identify and solve problems with RC tools. Focus is on practice application and creating a problem-solving culture.

  • August 31 - Sept. 4 | Daily 1:30 -  5:00 p.m. (EST)

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Design Control Training for Medical Devices

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

  • Sept 14 - 18 | Daily 1:30 -  5:00 p.m. (EST)

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