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

February 28-March 01, 2019 ANA Crowne Plaza |

Global Pharmaceutical and Pharma Industry Conference

Osaka, Japan
March 18-19, 2019

13th International Conference on Biosimilars and Biologics

Amsterdam | Netherlands
July 26-27, 2019

13th Asian Biologics and Biosimilars Congress

Mercure Albert Park | Melbourne, Australia

Clinical Trial Site Selection and Management Conference Speakers

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