The Clinical Patient Management System (CPMS) is a virtual consultation platform which enables healthcare professionals to present patient cases and collaborate with other healthcare professionals to provide diagnosis, care and treatment across borders. What are the European Reference Networks? There are over 6,000 rare diseases…
News
Digital and Central: Treat rare diseases through digital networking across institutions
OpenApp CEO, Con Hennessey, has been invited to speak about the Clinical Patient Management System (CPMS) at a the “Digital and central: Treat rare diseases through digital networking across institutions” online symposium. Launched in 2017, CPMS serves as a critical tool supporting the European Reference Networks (ERN) by facilitating…
“Ireland’s Commercial Open Source Ecosystem” Opportunities
How is Open Source driving innovation across global industries as well as within Ireland? Skillnet Ireland will be hosting their inaugural Open Source & Ireland’s Innovation Ecosystem Conference on Thursday, February 25th from 4-6pm GMT. The agenda is packed full of speakers who are experts on…
OpenApp Featured in Rare Revolution Magazine: Patient Registries - Myth vs Fact
We are delighted to inform you that we have featured in one of the foremost publications in the rare disease space. In the Autumn 2020 issue of Rare Revolution magazine we delve into some frequently asked questions regarding registries and use our expertise to debunk…
OpenApp Partnership with Specialisterne
As a pioneering software development company whose work affects the lives of thousands of people around the world, OpenApp remains extremely committed to matching the high standards of work we have set with a team of highly skilled employees. In order to help ensure this,…
Con Hennessy Interview With Rare Revolution Magazine
We are delighted to announce that our CEO, Con Hennessy, has been featured in esteemed rare disease publication Rare Revolution, in their “The People of Rare: CEO Series” campaign.The Rare Revolution “People of Rare” campaign aims to provide a glimpse into what drives the leaders…
OpenApp Exhibit at World Orphan Drug Congress
Last week the Client Engagement team and MD Con Hennessy attended World Orphan Drug Congress in Barcelona, Spain. Now in its 10th year, WODC has become one of the largest and well-established events on rare diseases and orphan drugs within Europe, catering for patient advocacy…
Building a rare disease patient registry
Con Hennessy of OpenApp was delighted to be invited to speak at the Findaure workshop – ‘Building a Rare Disease Patient Registry’. Rare Disease Registries are a well talked about initiative so it was great to see an organisation dedicate a full day workshop…
