Course overview
ISO 13485:2016, as an international standard for Quality Management System Requirements stipulated in the medical device industry, involves the design, development, production, installation and service of medical devices. Through the study of this course, students can understand the structure and requirements of ISO13485 Quality Management System. According to ISO 19011:2018 "Audit Management system Guide" to provide students with in-depth knowledge and skills in auditing. So that students have ISO13485 audit basic ability. Meet the requirements of ISO13485:2016 medical device quality management director auditor system director auditor.
The course meets the training requirement for Exemplar Global (TPECS) Auditor certification program for the below achievement.
- Exemplar Global – MD
- Exemplar Global – AU
- Exemplar Global – TL
Course purpose
The course meets the training requirements for Exemplar Global (TPECS) Provisional Auditor Certification for medical device.
Intertek Course advantage
- EG Authorized accredited courses
- Personally taught by the Chief Gold Training Provider
- Exclusive Gold Teaching Assistant Service
- More questions and practice sharing to ensure learning quality
Course Outline
- Overview of the Quality Management System (ISO13485 & ISO9001 background, principles, objectives, etc.)
- A brief description of the content and structure, scope, terms and definitions of ISO 13485: 2016
- Detailed analysis of ISO 13485:2016 standard terms.
- ISO13485:2016 Chief auditor knowledge and skills analysis (role, responsibility, ISO14971 risk management, regulations, etc.)
- Interpretation of ISO19011 audit guidelines (audit types, audit roles, audit schemes, audit planning, etc., auditor code of Conduct)
- Analysis and implementation of audit process and skills (preparation of audit plan and checklist, issue of non-conformance items; Audit principles, audit skills, audit methods and skills, simulation audit)
- Preparation and follow-up of audit report
Who should attend
- Individuals who want to obtain a formal qualification in the application of Medical Devices to add to their auditing experience
- Individuals leading their companies to ISO 13485 certification
- Business Managers, Quality Managers, Engineers, Compliance Officers, and Consultants
- Individuals who want to become a Certified Medical Device Quality Management Systems Auditor through their relevant certifying body such as Exemplar Global
Achievement
This course is certified by Exemplar Global under the TPECS scheme.Upon successful completion of this course and passing the examination, students will be granted Certificate of Attainment with the following Exemplar Global competency units
- Exemplar Global – MD – Medical Device Management Systems
- Exemplar Global – AU – Management Systems Auditing
- Exemplar Global – TL – Leading Management Systems Audit Teams
Course schedule
5 days
Course Time and Venues
Date and Time |
Location |
July, 22-26, 2024
*The specific time may be adjusted according to the registration situation. |
Shanghai, China
*The specific training venue will be informed before the start of the course according to the students' registration situation. |
Course Fees:
RMB 12,000 per person
Limited time discount, register as soon as possible
Please contact customer service representative for details.
更多信息请咨询:
邮箱联系:china.medical@intertek.com
欢迎垂询:021-5339 7737
Intertek
Intertek is a leading Total Quality Assurance provider to industries worldwide with professional, accurate, fast, passionate total quality assurance service, to win the market escort for customers.Our network of more than 1,000 laboratories and offices and over 44,000 people in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers’ operations and supply chains.
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