We attended & supported the @eupatientsforum, focusing on the further digital transformation of healthcare. Anca Toma, Executive Director of EPF, voiced key elements for sustainable digitalization: trust, consent, inclusiveness, collaboration & dialogue. #EPFcongress2022
The launch of our #PatientPartnership Charter is a crucial and tangible step forward in our journey to build deeper, long-term partnerships with the patient community. Read more in our Annual Report Magazine: https://t.co/PSz29PSyyv
#PioneeringForPatients
Proud and happy that Paul Stoffels will take over the CEO role at Galapagos. Paul is one of the world’s most successful leaders in the industry and also a co-founder of the company. This will be the turning point - welcome Paul!
“We are not just sitting here to let it take over. We’re fighting." For patients, caregivers are as essential as their physician. We asked Maxine, Ron’s wife & caregiver, how she sees a caregivers’ role when it comes to #ClinicalTrials. 👇 https://t.co/2NUsejvtYz
Patients are our North Star. Their needs guide everything we do. We are committed to working for patients, with patients.
📽️ Watch the video: https://t.co/xUndEnle6e
ℹ️ Discover more: https://t.co/agrU90TWMD
#ARmagazine#PioneeringForPatients
As #PFSUMMIT21 draws to an end, we’re delighted to have been part of this journey. At Galapagos, we believe that through partnership we can work together to improve PF care. Steve Jones @ActionPFsteve of @EU_IPFF agrees with this approach. Thank you for an inspiring summit. 🤝
Today at #PEOF, we'll cocreate the process of transforming @imi_paradigm "Patient Engagement Metrics Framework" into a customised tool for anyone working on a #patientengagement initiative. Check out session pre-reads & join us at 16:30 CET.
➡️ https://t.co/g8SlzYjnQU
It’s @RareDiseaseDay! We are proud to join @EURORDIS in supporting the courage, strength and resilience of the 300 million people living with #RareDiseases.
Watch what this day means to Ron, who lives with a rare & progressive disease #IPF
https://t.co/Q0JvBPte50
It’s @rarediseaseday week and we are looking forward to sharing an inspiring story of strength and resilience to support voices of the #RareDiseases patient community. Watch this space! #MyPFStory
"Patients’ emotions matter in the regulation of medicines" - take a look at recent opinion on considering the emotional (not only physical) impact of patients involved in regulatory affairs by EPF President Marco Greco and Natalie Bere of @EMA_News here: https://t.co/wMfrsFbmKJ
Research has shown that #RheumatoidArthritis can affect all aspects of a person’s life, including social relationships, family life, and psychological well-being.
Today, on #WorldArthritisDay, we recognize how crucial the patient voice is, and we commit to prioritizing what is important for people living with Rheumatoid Arthritis in their treatment and care. #PioneeringForPatients https://t.co/YWMwIfc2Zn
Someday just became today. Four simple words describe a complex yet exciting journey spanning over two decades. From a biotech start-up to an international biotech company, bringing innovative medicines to patients. #PioneeringForPatients
“There is an alarming variation in access to IPF care and management across Europe; urgent action is required”. Dr Francesco Bonella (@fratommy75), MD, Associate Professor at the Center for interstitial and rare lung diseases at @unidue. #ERSCongress#IdiopathicPulmonaryFibrosis