Daily Judi

Daily Judi: Tuesday, August 23, 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:

The European Commission announced Monday that it has approved Gilead’s new antiretroviral medication, Lenacapavir. Gilead markets this treatment as Sunlenca. The California-based Gilead designed Sunlenca as a twice-yearly dose, intended to block HIV at multiple stages. Reported by MedCityNews, Gilead Chairman and CEO Daniel O’Day said, “Following today’s approval, it will now be the only twice-yearly treatment for people who struggle with multi-drug resistant HIV.”

Clinical Leader spoke with Benchmark Research's Chief Business Officer, Cynthia M. Dukes, PA, MT, about the COVID-19 pandemic and the United States government’s response (Operation Warp Speed). Dukes discusses how the pandemic accelerated the speed of clinical trials and subject enrollment.

Meanwhile, at the BMJ, a comprehensive look at 255 randomized trials. Its authors provide a systematic review of the clarity of research questions.

The CNS Summit 2022 will be held in Boca Raton, Florida, on November 17–20. 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. More insight is provided in a recently posted experience video. Team Judi will be there!

Our Culture

“I’ve been at the company over seven years, and it’s been really cool to watch the company grow and continue to increase how we help our clients. One of the many things I like about my job is that it’s not always the same thing every day, because each client is unique. It makes every day interesting.

Judi is a platform. It’s an adjudication tool, but it’s also more. It’s a whole collaborative workflow process tool. It works with DSMB, Eligibility, anything.”

                     –Stephen, Lead Engineer

About Judi

Judi helps clinical trial teams around the world come together to seamlessly manage complex workflows, interactions and insights, allowing them to do their best work. 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: Tuesday, August 23, 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:

The European Commission announced Monday that it has approved Gilead’s new antiretroviral medication, Lenacapavir. Gilead markets this treatment as Sunlenca. The California-based Gilead designed Sunlenca as a twice-yearly dose, intended to block HIV at multiple stages. Reported by MedCityNews, Gilead Chairman and CEO Daniel O’Day said, “Following today’s approval, it will now be the only twice-yearly treatment for people who struggle with multi-drug resistant HIV.”

Clinical Leader spoke with Benchmark Research's Chief Business Officer, Cynthia M. Dukes, PA, MT, about the COVID-19 pandemic and the United States government’s response (Operation Warp Speed). Dukes discusses how the pandemic accelerated the speed of clinical trials and subject enrollment.

Meanwhile, at the BMJ, a comprehensive look at 255 randomized trials. Its authors provide a systematic review of the clarity of research questions.

The CNS Summit 2022 will be held in Boca Raton, Florida, on November 17–20. 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. More insight is provided in a recently posted experience video. Team Judi will be there!

Our Culture

“I’ve been at the company over seven years, and it’s been really cool to watch the company grow and continue to increase how we help our clients. One of the many things I like about my job is that it’s not always the same thing every day, because each client is unique. It makes every day interesting.

Judi is a platform. It’s an adjudication tool, but it’s also more. It’s a whole collaborative workflow process tool. It works with DSMB, Eligibility, anything.”

                     –Stephen, Lead Engineer

About Judi

Judi helps clinical trial teams around the world come together to seamlessly manage complex workflows, interactions and insights, allowing them to do their best work. 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.

Oncology
Partnership Success Story

Prominent clinical-stage biotech combines Judi for Eligibility and Judi for Adjudication on pivotal Phase 2 CAR-T oncology trial with over 600 endpoints

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Rare Disease
Partnership Success Story

International biopharma sponsor and partner CRO maximize flexibility of Judi for DSMB for Phase 2 multinational clinical program with over 100 patients and 60 sites

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Oncology
Partnership Success Story

US-based biopharma leverages scalability of Judi for Imaging on three concurrent pulmonary oncology trials

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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

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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