Daily Judi

Daily Judi: Friday, August 26, 2022

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:

Bloomberg reports that merger negotiations are stalled between Merck and cancer-drug maker Seagen (formerly Seattle Genetics, Inc.) If the deal goes through, it will be Merck's largest in more than ten years.

Clinical Leader details how to improve upon the common goal of prioritizing patient centricity across our entire ecosystem. Jeff Parke writes, "It is vital to promote dialogue, especially among people who may approach the issue from different perspectives. Only then can we overcome the current barriers."

Claudio Fiocchi and Dimitrios Iliopoulos discuss the challenges and need for developing more effective forms of treatments for inflammatory bowel disease. (Journal of Crohn's and Colitis)

Meanwhile, in the New England Journal of Medicine, C. Joseph Ross Daval, J.D., Aaron S. Kesselheim, M.D., J.D., M.P.H., and Ameet Sarpatwari, Ph.D., J.D., argue a consistent approach is needed in how the FDA uses its advisory committees.

The CNS Summit 2022 will be held on November 17–20, in Boca Raton, Florida. Created as "a community of innovators and industry leaders who are not afraid to challenge the status quo," CNS was founded in 2009 to advance clinical development, focused on collaboration and innovation. Team Judi will be there!

We also hope to see you this September 13-14, in Boston, for DPHARM: Disruptive Innovations to Advance Clinical Trials, walking distance from our North End headquarters.

Our Culture

“We create a template so we can pull back the timelines and eliminate concerns around quality and risk—because everything’s already validated in the design.
Then we can work faster with no risk to quality.”

                                             –Jamie, Trial Delivery

About Judi

Judi is on a mission to empower the ecosystems that drive clinical trial success by improving their workflows. We eliminate the chaos so clinical teams can focus on the patient, rather than the process. We are a SOC 2 Type II certified collaboration platform.

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Daily Judi

Daily Judi: Friday, August 26, 2022

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:

Bloomberg reports that merger negotiations are stalled between Merck and cancer-drug maker Seagen (formerly Seattle Genetics, Inc.) If the deal goes through, it will be Merck's largest in more than ten years.

Clinical Leader details how to improve upon the common goal of prioritizing patient centricity across our entire ecosystem. Jeff Parke writes, "It is vital to promote dialogue, especially among people who may approach the issue from different perspectives. Only then can we overcome the current barriers."

Claudio Fiocchi and Dimitrios Iliopoulos discuss the challenges and need for developing more effective forms of treatments for inflammatory bowel disease. (Journal of Crohn's and Colitis)

Meanwhile, in the New England Journal of Medicine, C. Joseph Ross Daval, J.D., Aaron S. Kesselheim, M.D., J.D., M.P.H., and Ameet Sarpatwari, Ph.D., J.D., argue a consistent approach is needed in how the FDA uses its advisory committees.

The CNS Summit 2022 will be held on November 17–20, in Boca Raton, Florida. Created as "a community of innovators and industry leaders who are not afraid to challenge the status quo," CNS was founded in 2009 to advance clinical development, focused on collaboration and innovation. Team Judi will be there!

We also hope to see you this September 13-14, in Boston, for DPHARM: Disruptive Innovations to Advance Clinical Trials, walking distance from our North End headquarters.

Our Culture

“We create a template so we can pull back the timelines and eliminate concerns around quality and risk—because everything’s already validated in the design.
Then we can work faster with no risk to quality.”

                                             –Jamie, Trial Delivery

About Judi

Judi is on a mission to empower the ecosystems that drive clinical trial success by improving their workflows. We eliminate the chaos so clinical teams can focus on the patient, rather than the process. We are a SOC 2 Type II 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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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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