Patient-Centric Clinical Trials
Generally accepted principles suggest that patient involvement should extend well beyond consideration as research subjects. Patients are key stakeholders in all aspects of trial design & execution. Patient-centric drug development also offers a huge opportunity to define meaningful outcomes from the patient perspective, as a way to ensure the needs and priorities of patient populations are reflected in research. Although efforts are made to control risks to clinical trial participants, some risk may be unavoidable because of the uncertainty inherent in clinical research involving new medical products. It's important, therefore, that people make their decision to participate in a clinical trial only after they have a full understanding of the entire process and the risks that may be involved.
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Patient-Centric Clinical Trials Conference Speakers
Recommended Sessions
- Bioethics and Regulatory Compliance
- Clinical Data Management and Analytics
- Clinical Operations & Project Management
- Clinical Research & Clinical Trials: Academic Perspective
- Clinical Supply Management
- Clinical Trial Forecasting, Budgeting and Contracting
- Clinical Trial Site Selection and Management
- Clinical Trials on different Diseases
- CRO, Sponsorship & Outsourcing for Clinical Trials
- Drug Discovery and Development
- Enrollment Planning and Patient Recruitment
- Future of Clinical Trials and Technology Innovations
- Globalization of Clinical Trials
- Innovations in clinical study designs
- Medical and Clinical Case Reports
- Medical Imaging in Clinical Research
- Patient-Centric Clinical Trials
- Pharmaceutical Sciences
- Pharmacovigilance and Drug Safety
- Research and Trials on Oncology and AIDS
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