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Online Virtual Instructor-Led Medical Device Training

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

Oriel STAT A MATRIX is known for our in-person workshops and hands-on activities, and we use an extensive toolbox to foster similar engagement and attention in our virtual classes. Our instructor and students interact in real time via our flexible, online learning platform, resulting in an engaging and real-class environment.

This is an ideal alternative to the typical classroom setting for quality and regulatory professionals who are unable to travel or who just prefer the convenience of attending a class without having to leave their own personal environment.

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 class times are either "Virtual (AM)" or "Virtual (PM)." AM classes run 8:30 a.m.-12:00 p.m. EST (3.5 hours per day). PM classes run 1:30-5:00 p.m. EST (3.5 hours each day). Virtual seminars are typically delivered across 4 or 5 days.

See our Virtual Learning FAQs »

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Upcoming Open-Enrollment Virtual Instructor-Led Classes

QMS Training for Medical Devices: FDA QSR & ISO 13485

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

  • May 18 - 22 | Daily 1:30  -  5:00 p.m. EST

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Updated! ISO 14971 Medical Device Risk Management Training

ISO 14971:2019 has been released! Get up to speed on how to keep your risk management state of the art.

  • April 13 - 17  - AM Session | Daily 8:30 - 12:00 p.m. EST
  • April 13 - 17 - PM Session | Daily 1:30 -  5:00 p.m. EST
  • May 4 - 8  - AM Session | Daily 8:30 - 12:00 p.m. EST
  • May 4 - 8  - PM Session | 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).  

Attendees who successfully complete this class and pass a final exam will earn both a certificate recognized by Exemplar Global as evidence of your competency as well as an Oriel STAT A MATRIX credential in assessing proficiency.

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.    

May 18 - May 22 AM SESSION (EST)

  • Week 1: May 18 - 22   | Daily 8:30 a.m. -  12:00 p.m. 
  • Week 2: May 26- 29   |  Tues - Thrus -  8:30 a.m. -  12:00 p.m. , Fri - 8:30 a.m. - 2:00 p.m.

May 18 - May 22 PM SESSION (EST)

  • Week 1: May 18 - 22   | Daily 1:30 -  5:00 p.m. 
  • Week 2: May 26- 29   | Tues - Thrus -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m.

June 1 - June 11 PM SESSION (EST)

  • Week 1: June 1 - 5   | Daily 1:30 -  5:00 p.m. 
  • Week 2: June 8 - 11  | Mon - Wed -1:30  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m.

Learn More or Register »


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. 

  • April 20 - 24 | Daily 1:30 -  5:00 p.m. EST
  • May 11 - 15 | 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.

Attendees who successfully complete this class and pass a final exam will earn a certificate recognized by Exemplar Global as evidence of your competency as well as an Oriel STAT A MATRIX credential in assessing proficiency.

This class is delivered across 5 days. 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.    

  • April 20 - 24 | Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. EST
  • May 4 - 8 Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. EST

Learn More or Register »


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.  

  • April 27 - May 1 | Daily 1:30  -  5:00 p.m. EST
  • May 11- 15 | Daily 1:30  -  5:00 p.m. EST

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Internal Auditing to MDSAP

Learn how to audit using the MDSAP process-based approach and the unique requirements for each participating country.

Attendees who successfully complete this class and pass a final exam will earn a certificate recognized by Exemplar Global as evidence of your competency as well as an Oriel STAT A MATRIX credential in assessing proficiency.

This class is delivered across 5 days. 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.    

  • April 27 - May 1 Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. (EST)
  • May 11- 15 Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. (EST)

Learn More or Register »


EU IVDR Transition Training 

Learn key changes between the IVDD and IVDR, how to make the transition,and best practices for transitioning.

  • May 4 - 8 | Daily 1:30  -  5:00 p.m. 

Learn More or Register »


Design Control Training for Medical Devices

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

  • April 6 - 10 | Daily 1:30 -  5:00 p.m.

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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.

  • May 11 - 14 | Daily 1:30 -  5:00 p.m.

Learn More or Register »

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