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The Swedish Medical Products Agency is responsible for regulation and surveillance of the development, manufacturing and sale of pharmaceuticals and other

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i-Medical. products. All devices manufactured and marketed by i-Medical® meet the requirements of EU medical devices directive 93/42/EEC of 14 June 1993, the amendments directive 2007 47 EC of 29 March 2007, the German Medical Product Act (MPG), are registered with regulatory authorities in Germany, and bear the CE mark.

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iMEDICAL offers specialized medical services. If you would like to make an enquiry about any of our services please call or complete the form below and we will contact you as soon as possible. Click here to search for Collection Centres in your State. Collection Centres.

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Bite-Sized Medical News Emphasizing Evidence-Based Medicine Written by Residents for Students, Residents, and Junior Physicians People who know me, know that I love evidence-based medicine! Vi har varit med i två poddar. Hör oss prata om livet, träning, tävling, äventyr och en hel del mat! Ät Färg Spring Berg! IEC 60601 Medical Electrical Equipment Classification: FAQs Posted by Rob Packard on October 26, 2013. IEC 60601 medical electrical equipment classification frequently asked questions are discussed in this blog. Disclaimer.