[account_shop_links]
Best Practices in Study Feasibility
$4,460.00 – $8,920.00
Licensing Options
- SINGLE-USER LICENSE
A Single-User License allows access to an individual user.
- ENTERPRISE-WIDE LICENSE
An Enterprise-Wide License allows access to all employees and sites within an organization.
Report Overview
One of the primary challenges to successfully completing a clinical study is estimating the medical, clinical, logistical, and regulatory feasibility of the trial. Within the clinical trial feasibility process, sponsors, CROs and sites evaluate the possibility of conducting a clinical trial within a specific geographic region with the overall objective of completing the project with targeted patients and within defined timelines and costs. Thorough feasibility analyses that implement best practices will assist sponsors in delivering successful site start-ups and trials with data from the right patients while finishing on-time and on-budget. ISR gathered opinions from key stakeholders—sponsors, CROs and sites—to identify the best practices within the feasibility analysis process.
What you will learn:
- The percentage of trials that require a feasibility analysis and whether the analysis is conducted in-house or outsourced
- Objectives for conducting a feasibility analysis and the data sources utilized and site selection strategies
- Awareness of feasibility analysis service providers, frequency of use and how well providers performed with respect to client expectations
How you can use this report:
- Implement the top techniques and innovations identified by sponsors and CROs for conducting a feasibility analysis
- Improve the accuracy of your own feasibility analyses by learning which characteristics and activities contribute to predictive feasibility estimate
- Understand the potential value to be gained by engaging a specialized feasibility analysis firm under specific circumstances
