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Welcome to the medical device e-learning website.

This website is for all those people wishing to understand more about the medical device regulatory frameworks primarily within Europe and how to address them.

If you are a Design Engineer, Regulatory affairs specialist, Quality Manager or just interested in how to address medical device regulations our e-learning solutions will meet your needs.

We are dedicated towards ensuring that our materials are unique, up to date and address your learning needs. In order to achieve this we provide you with tutorials, video case studies and interviews as well as downloadable reference materials, procedures and resources.

15/04/2010 - Pink Associates launch website

20/04/2010 - Current survey for QARA personnel in large organisations

27/04/2010 - Research into post market surveillance for multi national organisations

21/05/2010 - Pink Associates appointed by J&J to undertake Organisational research

28/05/2010 - Pink Associates conducting survey on industry current learning needs

01/06/2010 - Risk Management in Medical Devices Book published by Pink Associates

08/06/2010 - ISO13485 Auditing guides being developed

25/06/2010 - NEW CONTENT - An interview with Boston Scientific the role of RA in Development Engineering

31/07/2010 - NEW CONTENT - Power point presentation, Project Management in Device Design

01/08/2010 - NEW CONTENT - Power point and media for auditing Software development projects