Remote Auditing for Medical Device Companies

Internal Audit and Supplier Audits are essential for medical device companies to self-identify and mitigate risks. The COVID-19 pandemic has made this important task even more difficult due to travel restrictions. This webinar will provide insights into how to use remote auditing techniques to minimize the risk and maximize the benefits of conducting audits remotely.

In this webinar, we will discuss:

  • How remote auditing differs from on-site auditing
  • Effective planning to maximize benefits
  • Risk Analysis techniques for remote audits
  • Balance between Supplier Audits and Acceptance activities
  • A long-term strategy for auditing using remote techniques

Why You Should Attend:

Continuous Improvement starts with awareness of issues and opportunities. And without an effective internal audit program, management lacks awareness of the issues within their quality system. Management is blind to the gaps in the quality system and the risk that poses for the company. Even worse, management is blind to the impact on product quality and risk to the customer. It is essential to continue your audit activities, both internal and supplier, during the COVID-19 pandemic. This webinar will highlight ways to maintain your audit program while travel is significantly restricted.

Areas Covered in the Session :

  • Background
  • Audit process basics
  • Comparison of on-site vs. remote audit
  • Audit considerations
  • Interviewing impacts
  • Remote audit etiquette
  • Risk Analysis
  • Do’s and Don’ts
  • Long term plan
  • Remote audit strategy
  • Checklist

Who Should Attend:

  • Quality Systems Specialists
  • Document Control Specialists
  • Quality and Compliance Specialists
  • Auditors
  • Auditor Managers
  • Supplier Auditors
  • Supplier Managers
  • Training Specialists
  • CAPA Specialists
  • Quality/Compliance managers or directors for Medical Device companies
  • General Managers wanting to learn how to Management Review and expectations


Susanne Manz

Susanne Manz is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. She has a BS in Biomedical Engineering and an MBA from the University of NM. She earned her Black Belt and Master Black Belt certifications while at Johnson and Johnson.

Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality. Susanne has now established a consulting business with a mission to provide services to help medical device companies achieve world-class quality and compliance.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance