Bolstering Study Team Efficiency and Ensuring Compliance in Clinical Trials

Introduction Informed consent is a critical component of clinical trials, ensuring participant understanding and protection. The traditional paper-based approach often adds to the administrative burden and[...]

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Mitigating Subject Consenting Errors with eConsent: A Leap towards Efficient Clinical Trials

Informed consent is a crucial step in clinical trials, ensuring participants' understanding and agreement to participate. However, the traditional paper-based approach is often prone to errors,[...]

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Digitalizing Budget Negotiation: A Path to Expedite Clinical Trial Startups

Budget negotiation is a fundamental and often complex process in the initiation of clinical trials. Traditionally, this process is time-consuming and potentially contentious, often leading to[...]

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The Role of Cosmos Clinical eConsent in Reducing Consenting Errors

The process of obtaining informed consent for clinical trials is a critical element in ensuring the ethical conduct of research. The consent process is designed to[...]

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How to comply with the End of Study documents using COSMOS eVault

How to Comply with the End of Study Documents using COSMOS eVault A perfect End of Study (EOS) data exchange is critical for the successful closure[...]

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How eConsent helps the site

How eConsent helps the site and comply with the GCP Generally, informed consent (IC) is a process that educates a participant about all the aspects of[...]

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How to optimize the study startup (SSU)

Study Startup (SSU) – which encompasses various critical steps required to start a study – is an inherently complex process with typical roadblocks. Given that the[...]

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Expedite the study enrollment with Decentralized Trials

Expedite the study enrollment with DCT Decentralized Clinical Trials (DCT): Decentralized clinical trials (DCTs) are the focus point in many industry discussions and activities due to[...]

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