One-stop solution for every clinical case

With Maven CDMS® at its center, Maven Clinical Cloud consists of services essential for the most effective clinical trial operation.


With EDC as its cornerstone, Maven CDMS® provides various features and functions for clinical trial operational excellence.

Features

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Maven EDC: A cloud-based Clinical Data capture and monitoring solution

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Maven Trigger: Auto / Manual Query system

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Maven Coder: Medical coding with global medical and drug dictionaries

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Maven RTSM: IWRS-based randomization and IP management

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Maven Auditor/Auditor+: Blockchain-based audit trail

Value Proposition

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Hyper Connectivity: Integration with third party solutions for the most optimal data management

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Seamless Journey: Modular structure allows full customization to fit all clinical trial designs

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Data Secured: Tamper-free data protected by blockchain-based audit trail

Maven eCOA® is a web-based survey system to efficiently communicate with and collect data from subjects.

Features

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Accessibility: Easy access via a SMS-accessed web-based solution

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Identification: 3rd Party user verification options

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Customizability: Fully customizable questionnaires and surveys

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Connectivity: Real-time connection with Maven CDMS®

Value Proposition

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Improved Access: BYOD to increase user accessibility

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Enhanced Data Stream: Real-time and actionable data collection and monitoring

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Flexible Integration: Bespoke eCOA customizable with different scales, visuals, and methodologies

Maven Docs® is a clinical trial document management solution that accompanies a documents lifecycle from writing to reviewing and approving.

Features

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Composer: Documents standardization to simplify workflow and improve efficiency (PRT, ICF, MVR)

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Viewer: Secure and controlled document sharing

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Sign: Clinical trial ready embedded eSignature tool (21 CFR Part 11 compliant)

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Archiver: Easily store and access TMF

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Trainer: Provide LMS for study participants

Value Proposition

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Digital Assetization: Digitalization of clinical trial documents for sustainability and preservation

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Standardization: Templates allow a harmonized and controlled documentation for increased quality

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Process Simplification: Proprietary tools to simplify the document creation and management

Maven Safety® is a Pharmacovigilance solution for the management of Adverse Event from documentation and collection to exporting and agency reporting.

Features

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Ease of Input: Manual recording and Database migration

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E2B(R3)-compliant Agency Reporting: XML-conversion for reporting and Direct reporting via Maven Safety® systemComing Soon

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Blind / Unblind Option

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Review and Approval Process

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Block-chain based Audit Trail

Value Proposition

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Digital Assetization: Store and database AE for use during R&D and post-marketing

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Process Simplification: Cost-conscious solution that is E2B(R3)-ready


Qualifications

Your Partner for a Successful Journey

JNPMEDI has been putting effort on bringing disruption on healthcare industry via integrating digital technologies to clinical research & trial operations.