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Cloudbyz offers Clinical Trial Management on the Salesforce 1 cloud platform for sponsors, clinical research organizations (CRO), hospitals and medical centers. Cloudbyz CTMS is flexible and scalable to enable, manage and collaborate on clinical trial operations while the intuitive, straightforward design allows rapid deployment with a very intuitive and easy to use cloud based solution. Cloudbyz CTMS helps to manage sites, enrollment, documents, events, milestones, site visit reports, finances, inventory, etc.
Cloudbyz CTMS enables a centralized trial management database for all investigators, provides users with relevant and timely information, delivers trial information to clinical research associates and managers, enables clinical trial sponsors to collect and track all relevant data and facilitates communications to the study team.
The drag & drop functionality enables users to drag and drop one or more files from the laptop or desktop for uploading files to the desired eTMF folder, thereby ensuring best levels of flexibility.
Document approval feature helps in excluding manual paper handling tasks with automation in collecting, classifying, indexing and archival of email, medical images and docs, providing ideal results.
Document approval feature helps in excluding manual paper handling tasks with automation in collecting, classifying, indexing and archival of email, medical images and docs, providing ideal results.
Users could easily create documents for adverse events, protocol anomalies, trip reports and site green light process to save them on the eTMF platform at a single click for process documentation.
The drag & drop functionality enables users to drag and drop one or more files from the laptop or desktop for uploading files to the desired eTMF folder, thereby ensuring best levels of flexibility.
Document approval feature helps in excluding manual paper handling tasks with automation in collecting, classifying, indexing and archival of email, medical images and docs, providing ideal results.
Document approval feature helps in excluding manual paper handling tasks with automation in collecting, classifying, indexing and archival of email, medical images and docs, providing ideal results.
Users could easily create documents for adverse events, protocol anomalies, trip reports and site green light process to save them on the eTMF platform at a single click for process documentation.