Digital Healthcare Agency, Integrated Change, has launched a free 12 step guide to writing a mobile app brief for the healthcare industry. The 21 page document is intended to guide healthcare organisations considering developing a mobile application through the often under-valued step of writing the initial brief.
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Proceedings of the 6th International Advanced Research Workshop on In Silico Oncology and Cancer Investigation - The CHIC Project Workshop (IARWISOCI)
On November 3 - 4, 2014 the 6th International Advanced Research Workshop on In Silico Oncology and Cancer Investigation - The CHIC Project Workshop (IARWISOCI) was held in Athens, Greece. This IEEE-EMBS technically co-sponsored conference proved an excellent opportunity for contributing to the shaping and advancement of the emerging discipline of in silico oncology.
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Overview of the National Laws on EHR in the EU Member States and their Interaction with the Provision of Cross-Border eHealth Services
The objective of this Study is to provide an overview of the current national laws on electronic health records (EHRs) in the EU Member States and their interaction with the provision of cross-border eHealth services mentioned in Directive 2011/24/EU. This entails first to identify and examine the national laws of the 28 Member States and Norway and identify legal barriers for cross-border transfer data from electronic health records and for
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Health at a Glance: Europe 2014
European countries have achieved significant gains in population health, but there remain large inequalities in health status both across and within countries. Life expectancy at birth in European Union (EU) member states has increased by more than five years on average since 1990, although the gap between those countries with the highest and lowest life expectancies remains around eight years.
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Guidelines on ePrescriptions Dataset for Electronic Exchange under Cross-border Directive 2011/24/EU
These guidelines respond to Article 11 (2-b) of the Directive, which defines the need for "guidelines supporting the Member States in developing the interoperability of ePrescriptions". They are intended to be complementary to Commission Implementing Directive 2012/52/EU of 20 December 2012 laying down measures to facilitate the validation of medical prescriptions issued in another Member State (Implementing Directive 2012/52/EU).
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