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…

Findaure 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…

Live 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…

OpenApp 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…

Laois 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…

OpenApp 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…

OpenApp 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…

Launch 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…

Rare 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…