Understanding ISO 13485

ISO 13485:2016 • IN-PERSON WORKSHOP • LIVE VIRTUAL WORKSHOP

In this two-day training participants will learn the concepts of ISO 13485:2016 as well as gain a clause-by-clause understanding of the standard. This course is designed to provide you with insight into the use of ISO 13485:2016 as the basis for a quality management system implemented by medical device manufacturers, highlighting the value that implementation can bring your overall business management system.

Enrollment Options

Choose from our available Open Enrollment dates or request a private training session below.

Length

2 Days

Prerequisites

None

Demonstrate an understanding of the purpose and intent of the ISO 13485 standard
Define terminology and exclusion requirements in ISO 13485
Compare the requirements between ISO 13485 and ISO 9001
Interpret the clauses of ISO 13485
Recognize the role and responsibilities of management in ISO 13485
Appreciate the use of ISO 13485 as the basis of Medical Device Regulations worldwide
Recognize the relationship between ISO 13485 and ISO 14971

Senior Management, Quality Managers, Regulatory Affairs Managers, Internal and External Auditors, and anyone involved with the implementation of the standard.

Day 1

Purpose and Objectives
Process Approach and Impacts
Clause by clause review of ISO 13485

Day 2

Clause by clause review of ISO 13485 (continued)
Quality Management Principles
Closure and Planning: Opportunities, roadblocks and implementation planning

981-424-5348

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