TRAINING

The 2007-47 European Directive amended Directive 93-42 by introducing 2 new important concepts for medical devices (MD):

1) the medical device user profile
2) the user environment for the aforesaid MD

These 2 concepts, which were incorporated in the group's companies, have profound implications for the design of products and for the associated risk analyses.
Design must take the environment in which the medical device will be used into account (hospital, HEPAD, home, etc.) and reduce as much as possible the risks incurred from incorrect handling.
A good knowledge of the MD and its ergonomics by users (biomedical engineers, carers, patients, etc.) is therefore essential - in addition to design - for optimum risk management.

Winncare Services provides an inter-company training catalogue:

Winncare Services offers a complete range of training in the group's various products to take the requirements of the new Directive into account.
Several training levels and educational aids have been developed to satisfy user requirements.

Do you need training for one or more of your representatives?
Would you like a customised training programme suited to your structure and your requirements?
Would you like this training to take place at your premises to make the best use of your representatives’ time and to reduce costs?