Clinical Trial Site Selection and Management
Getting the correct outcomes from a clinical trial begins with picking the correct site as its prosperity is dictated by the clinicians who enlist, select, treat and assess trial patients. The experience of site staff, for example, agents or study organizers, the accessibility of reasonable patients and the capacity to perform required clinical evaluations are fundamental and must be considered while choosing a site. A regularly belittled process, site determination requires due constancy with respect to the support to guarantee the clinical trial meets all thought fundamental to the achievement of an examination. The accessibility of specific demonstrative and remedial gear, a reputation with past, comparable trials, the geographic area and administrative history must be considered in an indistinguishable way from authoritative and budgetary confinements and the expected rate of patient collection.
- Protocol development, site selection, feasibility and management
- Data-driven feasibility, country selection, and site identification
- Develop a technology road map for your research site
- Site management innovation
- Modernizing your Site
- Marketing & Business development for sites
- Financial management of research sites
- Regulatory inspections of research sites
- Strategies to validate the siteless trial
Related Conference of Clinical Trial Site Selection and Management
Clinical Trial Site Selection and Management Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Biopharmaceutical Sciences
- Clinical Data Management and Analytics
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Trial Protocols
- Clinical Trial Site Selection and Management
- Diversity in Industrial Clinical Trials and Clinical Research
- Drug Safety
- Drugs Regulations
- Good Pharmacovigilance Practice
- Hospital and Indutrial Pharmacy
- Medical and Clinical Case Reports
- Pre-Clinical and Clinical Trials