Understanding IEC/EN 60601-1 3rd Edition Requirements (1-Day) Training

Duration

1-day

Training Venue

WCCQ training centre in Kowloon Bay  (Hong Kong)

Language

Cantonese with Chinese / English materials

Description

Products come and go, and manufacturers and retailers who want a shelf life beyond the next holiday season must sell safe products. Brand image and reputation that have been carefully nurtured for years can be tainted in an instant. A large recall or a customer injury suit can wipe out in one stroke a multitude of merchant smart plays. To avoid such a crisis, there are numerous measures that Electrical and Electronic product suppliers need to consider, IEC/EN 60601-1 specific focus on medical. This is one-day training targeting to provide participants a understanding of the requirements in which the medical products should meet in order to minimize the risks of cost during the development period of products.

Learning Outcomes

To provide the IEC/EN 60601-1 requirements awareness training to enterprises, helping those companies what requirement of products on medical should meet in comprehensive way.

Course Content

- Overview of IEC/EN 60601-1 requirements

- Explanation of design requirements

- Overview of Amendment 1

Participants

Person are auditors of medical device manufacturers

Quality managers

Person are evolving in the development of medical devices

Learning Method

Lecture, case studies and assignment

Contact information

For further information or discussion on analyzing and meeting your training needs please contact us at certificates@wccq.org or (852) 2110 8492.

Remarks

# Onsite training Quotation only: please contact us for an on-site proposal. We respond to inquiries on the same day.