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CLINICAL TRIAL GLOBAL INSURANCE GUIDE
As an experienced clinical researcher, I understand the critical importance of navigating the complex landscape of global insurance requirements for clinical trials. Ensuring proper indemnification and coverage is not only a regulatory necessity but also a fundamental aspect of safeguarding the well-being of study participants and the integrity of the research itself. In this comprehensive guide, we will delve into the intricacies of clinical trial insurance, exploring the purpose, key components, and the global landscape of insurance requirements. We will also discuss strategies for navigating the challenges, managing risks, and ensuring a robust insurance strategy for your global clinical trials.
MASTER SERVICE AGREEMENTS
Line by line clarification of budget line items and considerations for Master Service Agreements. Can be integrated into your organization or purchased as a full guidebook that includes a template MSA and Budget in Digital Format. This granular guide breaks down all considerations, including formulation, manufacturing, combo ingredient variables and more providing transparent insight into what components make a trial MSA.
eINFORMED CONSENT
Be a trailblazer in patient centricity by offering clinical trial prospective enrollees an immersive, visual, digital informed consent. Give our trial sites the ability to offer a website or mobile application to review the informed consent and the transparency to reference at any time with family for informed decision making.