Medical Device Single Audit Program (MDSAP): Fundamentals and Readiness

Gain the knowledge and skills required to successfully host a MDSAP audit within your organization.

Obtain in depth knowledge about this new type of audit and how your organization is best prepared to support the completing of requirements within the allotted time. 

Discover how this program differs from the traditional ISO 13485 through its regulatory audit approach, the grading of nonconformities, and handling of the audit report. This course will prepare you to host a MDSAP audit and allow you to determine if your own internal QMS processes are consistent with the requirements of the MDSAP audit mode for the jurisdictions where your products are marketed.

Upon completion of this training, delegates will be able to support their organization to maintain compliance to ISO 13485 and jurisdiction requirements in the countries engaged in the MDSAP program.


Who should attend?

Quality Assurance and Regulatory Affairs professionals within medical device organizations currently active in participating territories and organizations expanding their market reach to jurisdictions participating in MDSAP.

Prerequisites
Delegates will benefit from reviewing the MDSAP Companion Document and ISO 13485:2016 standard before attending this course.

By the end of this course delegates will have the:

Knowledge to: 

  • Demonstrate awareness of MDSAP fundamentals
  • Explain the structure and scope of the MDSAP audit program:
    • MDSAP audit processes and their interrelationships
    • MDSAP and organizational regulatory compliance
    • MDSAP reporting and nonconformity grading
  • Explain the differences between MDSAP and other QMS audits
    • MDSAP and auditing in the medical device industry
    • ISO 13485 and ISO 14971
  • Identify MDSAP documentation

Skills to:

  • Prepare to host a sucessful MDSAP audit:
    • MDSAP 7 auditing process requirements
    • Plan audit scopes
    • Analyze data sources required during process audits
    • Analyze control interactions
    • Use correct jurisdictional terminology

How will I benefit?

This course will help you:­­­

  • Improve auditing skills focused on regulatory auditing
  • Improve competence for MDSAP internal auditors and the support needed to host a MDSAP audit
  • Assess your own audit models and suggest improvement
  • Be prepared to support an efficient MDSAP audit by your selected Auditing Organization

Practical information

  • It's a 2-day course
  • The training and the materials will be provided in English.
  • Lunch and drinks are included.

 

For further information regarding reduced rates at the hotel where the training is being conducted please contact training.nl@bsigroup.com or call 0031-(0)20-3460780.


Course Guide

In company

We can deliver this training course to your team in-house. Training in-company allows you to save on each individual delegate and also cut out travel and accommodation expenses, which can be significant.With our in-company training, not only can you meet your business needs, but you can also:

  • Refresh your team’s skills and boost their confidence
  • Give your team an overview of your management system(s)
  • Train a group of auditors to the same level, using the same consistent techniques

For more information about the in-company training or to request a quote, please contact Mark Leenaers via +31 (0)20 346 07 83 or send an email to mark.leenaers@bsigroup.com

 

Download the Medical Device Single Audit Program (MDSAP) Fundamentals and Readiness Training Course Guide.