Research and Drug Development

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Patient Engagement Resource Center

Published by EATRIS

Patient EngagementPatient InformationResearch and Drug Development

The Patient Engagement Resource center is an easy to navigate platform to help researchers get started with patient engagement in research. This toolbox provides helpful resources to help researchers understand the basics of patient engagement, and guide them through the different phases of patient engagement, from planning to conducting and evaluating.

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Stakeholders interactions – Patients Affairs Staff

Published by IRDiRC

Research and Drug DevelopmentRegulatory AffairsClinical DevelopmentEarly Access SupportPatient EngagementPatient AdviceFDA Regulatory AdvicePatient Affairs StaffPatient Support

At the FDA, the Patient Affairs Staff (PAS) is devoted to supporting cross-cutting patient engagement activities across the FDA. Its mission is to coordinate and support patient engagement activities across FDA to facilitate awareness and collaboration with patients, their advocates and the FDA

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Feasibility-Patient engagement in trial endpoint selection 

Published by IRDiRC

EndpointResearch and Drug DevelopmentClinical DevelopmentPatient EngagementClinical TrialOutcome MeasureTrail Endpoint Selection

Guidance on the pivotal clinical trials outcomes measures .The important of the patient’s feedback. Academics can then assess whether there is an outcome measure available that can measure this – if not, outcome measure(s) may need to be developed.

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