Daily Judi

Daily Judi: Friday, March 3, 2023

Every day we scan the headlines for the best items that engage the clinical trial ecosystem, workflow solutions, and more—all the latest news you need to know. Here are today's stories:

Yesterday, Novo Nordisk announced it will expand research and development lab facilities in the metro Boston region, which will create over 200 jobs. (BioPharma Dive)

Attorneys Michele Buenafe, Jake Harper, and Andrew Gray, examine current U.S. Food and Drug Administration regulations concerning AI in medical devices. (Med Device Online)

New Hampshire epidemiologist Dr. Benjamin Chan reflects on three years of the COVID-19 pandemic. (WMUR)



Our Culture

“I work mainly with one CRO, and they thank us for being proactive, and for our precise attention. We get a lot of appreciation from their whole team as we help them with their deliverable.”

   –Jess, Program Manager



About Judi

Judi speeds and improves the world's clinical trial workflows. Our cloud-based platform has 120,000 users across 171 countries. We eliminate the chaos so clinical teams can focus on the patient, rather than the process. We are a SOC 2 certified collaboration platform.

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Daily Judi

Daily Judi: Friday, March 3, 2023

Every day we scan the headlines for the best items that engage the clinical trial ecosystem, workflow solutions, and more—all the latest news you need to know. Here are today's stories:

Yesterday, Novo Nordisk announced it will expand research and development lab facilities in the metro Boston region, which will create over 200 jobs. (BioPharma Dive)

Attorneys Michele Buenafe, Jake Harper, and Andrew Gray, examine current U.S. Food and Drug Administration regulations concerning AI in medical devices. (Med Device Online)

New Hampshire epidemiologist Dr. Benjamin Chan reflects on three years of the COVID-19 pandemic. (WMUR)



Our Culture

“I work mainly with one CRO, and they thank us for being proactive, and for our precise attention. We get a lot of appreciation from their whole team as we help them with their deliverable.”

   –Jess, Program Manager



About Judi

Judi speeds and improves the world's clinical trial workflows. Our cloud-based platform has 120,000 users across 171 countries. We eliminate the chaos so clinical teams can focus on the patient, rather than the process. We are a SOC 2 certified collaboration platform.

Case Study
A Unique Solution for Patient Eligibility Review

Leverage Judi for increased compliance: expedited, high quality, structured decision-making on centralized patient eligibility determination that can eliminate an entire category of important protocol deviations from your trial

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Case Study
Judi for Remote Monitoring and Medrio EDC Integration

Prominent international biotech partners with Judi by AG Mednet and Medrio for holistic solution to remote monitoring and electronic data capture (EDC) on three-year global clinical program of 10 studies

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Whitepaper
Navigating the Post-Capture Era of Clinical Trials

From Data Capture to Data Liberation

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Daily Judi

Adjudication

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Imaging

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Eligibility

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Monitoring

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DSMB

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Qualification

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Key Benefits for
Daily Judi
Trials

Key Features

Workflow

Create customized workflows per event type, even within a single protocol or program

Electronic Case Report Forms

Enable eCRFs with advanced edit checks and data validation capabilities at any point in the process

De-Identification

Integrated tools enabling removal of protected health information (PHI) from document submissions

Query Management

Manage all event-related queries within the system and keep a log of all interactions

Notifications

Advanced email and web-service notifications to users based on their role

Audit Logging

Robust and compliant audit logging of all actions within Judi

Medical Imaging

Upload, de-identify, store and review medical images as part of endpoint or event submission

Role-to-Role Communications

Specific roles or groups to chat about a case or a project, detailed audit log of all interactions

Robust Reporting Infrastructure

Library of commonly-used reports to provide visibility to a given project’s status or status across a number of projects in a program. Ad hoc reports.

Dashboards and Worklists

Standard and customizable dashboards to help users visualize worklists, case status and project health

Integration

Communicate with EDC and safety systems through a well-defined web-services API

AI-Assisted Redaction

Judi’s proprietary AI-Assisted Redaction capability automatically detects potential inclusions of PHI and flags them for review, saving time and reducing regulatory risk.

Stay up-to-date with whats happening

Some sub copy covering what weekly/monthly update sand news one can expect.

Workflow

Create customized workflows per event type, even within a single protocol or program

Electronic Case Report Forms

Enable eCRFs with advanced edit checks and data validation capabilities at any point in the process

De-Identification

Integrated tools enabling removal of protected health information (PHI) from document submissions

Query Management

Manage all event-related queries within the system and keep a log of all interactions

Notifications

Advanced email and web-service notifications to users based on their role

Audit Logging

Robust and compliant audit logging of all actions within Judi

Medical Imaging

Upload, de-identify, store and review medical images as part of endpoint or event submission

Role-to-Role Communications

Specific roles or groups to chat about a case or a project, detailed audit log of all interactions

Robust Reporting Infrastructure

Library of commonly-used reports to provide visibility to a given project’s status or status across a number of projects in a program. Ad hoc reports.

Dashboards and Worklists

Standard and customizable dashboards to help users visualize worklists, case status and project health

Integration

Communicate with EDC and safety systems through a well-defined web-services API

See Judi in Action; Request a Demo today

Contact us today to learn more about how Judi can automate, expedite, and improve your clinical trials.

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