Learning Marketplace

Medical Device Single Audit Program (MDSAP) Fundamentals and Readiness Training Course

Course aim

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

Course description

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.

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

What will I learn?

Upon completion of this training, delegates will have the

Knowledge to:

  • Demonstrate awareness of MDSAP fundamentals
  • Explain the structure and scope of the MDSAP audit program:
  • 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

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.


2 days

How will I learn?

Our high impact accelerated learning approach increases learning by improving knowledge retention and skill application. This course is activity-based, resulting in a deeper understanding of the material and a greater impact on job performance.

What will I gain?

On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.


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

Further information:

Detailed course notes provided.

Related training:

You may also be interested in attending our ISO 13485:2016 series of courses (including internal and lead auditing).

Upcoming Course Dates

The venues for scheduled courses are tentative until receipt of course confirmation from BSI.

Start/End Date and Time Location Fee Enroll
  • Dec 09, 2019 8:00 AM - 5:30 PM
  • Dec 10, 2019 8:00 AM - 6:30 PM
San José, CA
Biltmore Hotel and Suites
2151 Laurelwood Road
Santa Clara, CA 95054
United States
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USD $1900.00Enroll
  • Jan 27, 2020 8:00 AM - 5:30 PM
  • Jan 28, 2020 8:00 AM - 6:30 PM
Boston, MAUSD $1900.00Enroll
  • Feb 10, 2020 8:00 AM - 5:30 PM
  • Feb 11, 2020 8:00 AM - 6:30 PM
San Diego, CAUSD $1900.00Enroll
  • Mar 16, 2020 8:00 AM - 5:30 PM
  • Mar 17, 2020 8:00 AM - 6:30 PM
Minneapolis, MNUSD $1900.00Enroll
  • Apr 06, 2020 8:00 AM - 5:30 PM
  • Apr 07, 2020 8:00 AM - 6:30 PM
San José, CAUSD $1900.00Enroll
  • Jun 01, 2020 8:00 AM - 5:30 PM
  • Jun 02, 2020 8:00 AM - 6:30 PM
Princeton, NJUSD $1900.00Enroll