patientMpower is looking forward to attending the European Respiratory Society (ERS) Congress, which this year is being held in Paris from 15 – 19th September.
We invite you to meet with us at ERS to learn more about our specialist remote patient tracking platforms for pulmonary fibrosis and lung transplant and our Digital Biobank of patient data.
The patientMpower mobile platforms for pulmonary fibrosis and lung transplant enable patients to track data relating to their pulmonary conditions remotely, using integrated monitors, and share this data in real time with their healthcare team. The information collected via the platform feeds into our Digital Biobank of real-life patient data, which is a unique resource for researchers, pharmaceutical companies and healthcare planners.
Come and have a chat with us to see how the patientMpower platform can help you with patient monitoring or how our real life patient data can be used in your research projects. To set up a meeting don’t hesitate to contact us at the email address below and come along to our poster session on the long-term use of the patientMpower platform in patients with pulmonary fibrosis.
Dr Colin Edwards, Chief Scientific Officer patientMpower: firstname.lastname@example.org
“Sustainability of use of an electronic health journal (patientMpower) for pulmonary fibrosis in a US patient support group (PF Warriors) over 180 days (poster PA4810)”
Tuesday 18th September at 12:50-14:40. Session TP45/466: “Back to basics and translational research in idiopathic interstitial pneumonias.”
by Eamonn Costello