Traditionally, health data has been generated by documenting patients’ records (i.e. clinicians’ notes, lab results, prescriptions etc.) in a paper-based system. However, this system has several challenges such as...
The development of Medical Devices should involve patients and the public throughout each stage: innovation, assessment, implementation and evaluation.This is essential in order to ensure that Medical Devices address...
Discover why patients’ voices matter by following David, Dimitrios, and Jan and how they have a voice in medicines R&D. How can EUPATI play a role to help patient...
Transcription So my name is Virginie Hivert, I’m working for EURORDIS, the European organisation for rare disease patients. I’m the Therapeutic Development Director, and so I’m a patient...
Introduction RWD and RWE are defined by the European Medicines Agency (EMA)[2] as a regulatory authority as such: RWD: “routinely collected data relating to a patient’s health status or...
Transcript My name is Matthew May. I work for DIA, which is a non-profit in the pharmaceutical industry. We’re a global membership association who also provide conferences and...
Transcription My name is Luís Mendão. I’m Portuguese, 58. I live with AIDS. I was until recently co-infected with hepatitis C. Hepatitis C was a very advanced liver...
Transcription Of course, my name’s Ross Carroll. I’m the Public Affairs Director for the UK and Ireland for UCB pharma. Within that role, I’m responsible for government affairs, for...
Transcription My name is Souzi Makri, I come from Cyprus. I’m an expert patient, I’m involved with the Cyprus League Against Rheumatism. I’m a member of the board,...
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