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Local standards and regulations are important considerations when developing assistive technologies.  While they can appear extremely complex, in reality they may be simpler than you first think.

Course aim:

Complimenting our CAD in AT range of courses, this session will develop your knowledge of the assistive technology regulatory framework in the UK/EU and the applicable relevant British, European and International Standards. We will cover key pieces of regulation and the primary standards that apply.

You will learn:

• How standards are developed and the standards hierarchy
• Relevant British, European and international standards including ISO 13485 (Quality), BS EN 12182/BS EN ISO 21856 Assistive products and the standards covering specific types of assistive technology
• The current and future regulatory framework in the UK and EU around Medical Devices
• Consumer protection legislation
• Testing
• Contributing to standards development

Course includes:

A live, interactive webinar will be run using Microsoft Teams.

Suitable for:

The CAD in AT series has been developed for makers, designers, engineers and others involved in the development of assistive technologies.

Max 20 participants

IPAACKS competencies:

Management of Resources

• Aware of legal and policy frameworks in reference to correct and safe use of AAC equipment (e.g. Medical Device Directives, Risk Assessments etc.)
• Knowledge of how to create resources to support the safe use of AAC technology

Special requirements:

You will need to use Microsoft Teams for the live online training. You will need to access online resources and Ace Centre Learning using a web browser.

Cost: £30 This is an introductory offer

Time:

• 18^th October 2022, 13.30 – 16.30  UTC +1 (Live online study)