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

Level Understanding Duration 2 days

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This two day course will help you to prepare 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 model for the jurisdictions where your products are marketed. On completion of the 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

On 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 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 successful MDSAP audit:
  
  MDSAP 7 auditing process requirements
  
  Plan audit scopes
  
  Analyze data sources required during process audits
  
  Analyze control interactions
  
  Use correct jurisdictional terminology
Quality Assurance and Regulatory Affairs professionals within medical device organizations who need to transition their CMDCAS certifications and organizations expanding their market reach to jurisdictions participating in MDSAP
This training course is HRD Corp claimable programme.
On completion, you will be awarded an internationally recognized BSI Training Academy certificate.

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