ISO 13485 Internal Audit Training Course

Our ISO 13485 Internal Audit Training Course focuses on both the requirements of ISO 13485:2016 and the audit process and methods (ISO 19011) to ensure the manufacturer or supplier is compliant with the requirements of the standard. Our approach is to educate on the intent and purpose of the standard so that the participants are able to make informed decisions in the future. Our training is helpful for regulatory, quality, production, and engineering roles, both management and contributors.

The current standard format course covers the topics listed below:

  • Quality terminology
  • Management responsibility
  • Resource management
  • Product realization and relationship to design controls, usability, cybersecurity, and software lifecycles
  • Purchasing
  • Production and service provision
  • Control of monitoring and measuring devices
  • Measurement, analysis, and improvement
  • Control of non-conforming product
  • Analysis of data and improvement
  • Principles of auditing
  • Managing an audit program
  • Preparing for audit activities
  • Conducting audit activities
  • Audit reporting clause
  • Completing the audit
  • Audit follow-up
  • Selection and training of auditors
  • Practical, real-world examples and discussion
  • Workshops and exercises integrated throughout teaching modules

Full credentials on our website:  https://www.softwarecpr.com/consultation/

This course can be provided live, onsite or remotely (requires camera on for entire course).

COST: 3 Full Days (9:00 am to 4:30 pm) for $21,000 for up to 21 students.  Extra cost per student over 21.

Course tailoring available for a fee.

To schedule the course or have a discussion, please email us at:  training@softwarecpr.com

About the author

Partner and General Manager, Brian Pate is ISO 1385:2016 Lead Auditor certified for Medical Device Quality Management Systems (MD), and ISO 19011:2018 Management Systems Auditing (AU) and Leading Management Systems Audit Teams (TL). Brian started his medical device career in anesthesia clinical research in 1985 and has since worked both academia and industry including many years with Johnson & Johnson, Baxter Healthcare, and GE Medical. Brian’s roles have included software engineering, systems engineering, quality assurance, and regulatory affairs. Brian has served on multiple AAMI TIR working groups, including TIR32-2008 (Application of ISO 14971 Risk Management to Software; now IEC 80002-1) and TIR45-2012 (Guidance on the use of Agile practices in the development of medical device software) and served as a reviewer for the 2nd edition of TIR45. Brian serves on the AAMI Software Committee and as an AAMI instructor for the software, design controls, and agile methods courses. Brian also is a member of the Underwriters’ Laboratories (UL) Standards Technical Panel for UL1998 (Software in Programmable Components) and or UL5500 (Remote Software Updates).

SoftwareCPR Training Courses

ISO13485:2016 ISO 13485 Internal Audit(or) Training Course (Live, 3-day)

IEC 62304 and other Emerging Standards Impacting Medical Device Software (Live, 3-day)

Being Agile & Yet CompliantISO 14971 SaMD Risk Management

Software Risk Management

Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.