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[...]
Read MoreHow 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[...]
Read MoreHow eConsent helps the site and comply with the GCP Generally, informed consent (IC) is a process that educates a participant about all the aspects[...]
Read MoreStudy Startup (SSU) – which encompasses various critical steps required to start a study – is an inherently complex process with typical roadblocks. Given that the[...]
Read MoreExpedite 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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