Insights
Catch the latest news relating to OpenApp here. This page is dedicated to Informative blogs covering such topics as the steps to set up a registry, importance of real world data, Resources to find out more about our products and how they can serve you, And our News section so you can see keep up to date with OpenApp’s press coverage

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. 21.11.2019 Now in its 10th year, WODC has become one of the…
Read MoreFindaure workshop – ‘Building a Rare Disease Patient Registry’.
Building a Rare Disease Patient Registry 18.09.2019 Con Hennessy of OpenApp was delighted to be invited to speak at the Findaure workshop – ‘Building a Rare Disease Patient Registry’. Rare…
Read MoreLive Webinar – Best Practices from Multiple Patient Registry Implementations
You are Invited to… ERN Population Registry Demonstration & Discussion Here are the Details for This Webinar: Due to the success of the last webinar, OpenApp are delighted to host…
Read MoreOpenApp Celebrates 17th Birthday
OpenApp Celebrates 17th Birthday As we close the door on another April, the leadership team in OpenApp decided to take a moment to celebrate it’s birthday. It was back in…
Read MoreLaois Ladies Gaelic Football Association and OpenApp Extend Sponsorship Deal
Laois Ladies Gaelic Football Association and OpenApp extend sponsorship deal In 2016, Laois LGFA & OpenApp were delighted to announce a new three year sponsorship agreement. This January, OpenApp and…
Read MoreOpenApp take home the Excellence in CSR by an SME Award in Corporate Social Responsibility Award 2018
OpenApp take home the Excellence in CSR by an SME Award in Corporate Social Responsibility Award 2018 OpenApp has been awarded the Excellence in CSR by an SME in the…
Read MoreOpenApp Develops Ground Breaking Platform Which Delivers Better Care to Rare Disease Patients
OpenApp Develops Ground Breaking Platform Which Delivers Better Care to Rare Disease Patients European clinicians treating over 30 million people who suffer from rare and complex diseases are reaping the…
Read MoreLaunch of Patient Registry for Pulmonary Lung Fibrosis
Launch of Patient Registry for Pulmonary Lung Fibrosis To enable monitoring of the standards of patient care and benchmark these against optimal diagnostic and care pathways, the Irish Thoracic Society…
Read MoreRare Disease Specialists across Europe Collaborating Online – how it works
Want to know more about the ERNs? On 1 March the newly established European Reference Networks (ERNs) began their work. ERNs are unique and innovative cross-border cooperation platforms between specialists…
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