May 10, 2023 - Cosmos Clinical

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[...]

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

Purna Cheekati May 10, 2023 eConsent

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,[...]

Digitalizing Budget Negotiation: A Path to Expedite Clinical Trial Startups

Purna Cheekati May 10, 2023 SSU

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[...]

The Role of Cosmos Clinical eConsent in Reducing Consenting Errors

Purna Cheekati May 10, 2023 eConsent , Regulatory

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[...]