The process by which clinical trial agreements (CTAs) are developed often has a tremendous impact on study start-up – affecting site-level budgets, payment terms, and Clinical Trial Management Systems (CTMS) set-up. There are many challenges involved in executing global CTAs and, in turn, performing investigator payments in clinical research, but a number of these challenges can be averted with proper planning and execution in the budget development stage.
Read this white paper to understand the most important considerations for a fully-integrated process that results in high-efficiency enabled contracts and payments.
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What You'll LearnMost Recent Flipbooks
Finding New Solutions to a Current Unsustainable Model of Clinical Trial Contracts & Budgets
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