We are happy to announce that we have added more information on the regulatory status of standards and that the graphical time evolution per standard now reflects the nationally adopted versions of international standards to normScan V.3.1.
normScan can now also indicate standards referenced by the FDA, and monitor these on a monthly basis alerting you by email to any changes.

For further insights, normScan also now offers three sub-tabs per standard; properties, attachments and the evolution.

If you would like to learn more about normScan and how it can help you monitor standards, please click here or contact us directly at .(JavaScript must be enabled to view this email address).
Each month the normScan newsletter alerts companies with the goings-on in the regulatory world.
To view this month’s newsletter, click here.
.(JavaScript must be enabled to view this email address) for an overview of the medical device standards information relevant to your complete portfolio.
Mireille De Cré and John Brennan
The European legislation which governs medical devices is undergoing continual evolution and this article analyzes and highlights the importance of all stakeholders’ participation in standards development.
Please click here to view this article.
Please note that this article first appeared in the June 2011 issue (volume 3, number 3) of the Global Forum and that copyright to this article is held by the DIA.