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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 Public Virtual Instructor-Led Classes

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. 

  • June 8 - 12 | Daily 1:30 -  5:00 p.m. EST

Learn More or Register »


EU MDR Auditor Training 

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

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.    

  • June 15 - 19 Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 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".

  • June 22 - 26 | 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.

  • June 1 - 5  | Daily 1:30  -  5:00 p.m. EST
  • June 22 - 26 | 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.    

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.

June 15 - June 25 PM SESSION (EST)
>> 
Week 1: June 15 - 19   | Daily 1:30 -  5:00 p.m. 
>> 
Week 2: June 22 - 25  | Mon - Wed -1:30  -  5:00 p.m., Thurs - 11:30 - 5:00 p.m.

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.  

  • June 8 - 12 | Daily 1:30  -  5:00 p.m. EST 

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EU IVDD to IVDR Transition Training (EU IVDR 2017/746) 

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

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

Learn More or Register »


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.

  • June 29 - July 2 | Daily 1:30 -  5:00 p.m.

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Medical Device CAPA Program Training 

Learn how to optimize your CAPA program by addressing common issues at the program level, the action level, and the problem level.

  • May 26 - 29 | Daily 1:30 -  5:00 p.m.
  • June 29 - July 2 | Daily 1:30 -  5:00 p.m.

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Medical Device Supplier Quality Management Training

Best practices and tools to manage a comprehensive, risk-based, cross-functional supplier quality management system.

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

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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.

  • June 15 - 19 | Daily 1:30 -  5:00 p.m.

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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.

  • June 8 - 12 | Daily 1:30 -  5:00 p.m.

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Design Control Training for Medical Devices

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

  • June 15 - 19 | Daily 1:30 -  5:00 p.m.

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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.

  • June 22 - 26 | Daily 1:30 -  5:00 p.m.

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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. 

  • June 1 - 5 Mon - Thurs -1:30  -  5:00 p.m., Fri - 11:30 - 5:00 p.m. EST

Learn More or Register »


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.

  • June 29 -  July 2 Daily 1:30  -  5:00 p.m

Learn More or Register »


Conducting A Remote Medical Device QMS Audit 

In this new virtual instructor-led training 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.

Learn More or Register »

Get answers right now. Call 1.800.472.6477

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