ISO 13485 – Medical Device Quality Management Systems

ISO 13485 is the international quality management system standard for medical devices.  The function of this standard is to “specify requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.”  The standard has its beginnings in ISO 9001 but as a standalone standard, it has evolved over the years through various versions.  

We will begin this webinar by overviewing the quality management system concept extended to both the QSR and the ISO standard to provide a solid and appropriate background to the further discussion of the standard.

We will next discuss the overall intent and impact of ISO 13485 in terms of why it is important and what it is intended to accomplish.

Once those basic concepts are overviewed the contents of the standard, and the impact of the various revisions and their specific change focus up to and including ISO 13485:2016.

We will spend some time discussing the differences between 21 CFR820 and the ISO Standard to fully realize the concept of conformance versus compliance.

We will end this webinar by discussing the process of implementing your quality system in conformance with the standard.

Why You Should Attend:

ISO 13485 is a standard and not a regulation.  In the US, it is vital to understand the differences between a standard and a regulation to avoid serious compliance failures.  That said, the standard is just that, a standard, and is the standard of choice for medical device manufacturers as it pertains to their quality management system.  Certification under this standard is essential to the organization’s ability to conduct business in the various markets that require conformity to this standard and compliance to its country’s regulations.

The ISO standard is also a valuable tool to the establishment, maintenance, and execution of the organization’s QMS as long as any variances to existing country regulations are understood i.e. the difference between a regulation and a standard.  This webinar will establish that foundation.

Areas Covered in the Session :

• Overview/basic elements of the quality management system
• Typical quality system elements
• Key attributes of a functional quality system
• QSR vs ISO Compliance
• ISO 13485 content overview and evolution of revisions
• Implementing your quality system in conformance with the standard

Who Should Attend:

• Quality Assurance Departments
• Quality Control Departments
• Regulatory Affairs and Compliance Departments
• Manufacturing Departments
• Production Departments
• Research & Development Departments
• Engineering Departments
• Operations Departments
• Logistics and Supply Chain Departments
• Service and Maintenance Departments

Course Director: CHARLES PAUL

Charles Paul is an instructional designer and management consultant with over 30 years’ experience providing training and consulting services to regulated industries. He has installed quality systems and designed and developed GMP and operational documentation and training programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.