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Clinical Research IO
Clinical Research IO

Clinical Research IO

By Clinical Research IO


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Highlights : About Clinical Research IO

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21 CFR Part 11 Compliance

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Electronic Data Capture

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HIPAA Compliant

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Patient Database

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Document Management

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Enrollment Management

About Clinical Research IO

Clinical Research IO is an intuitive e-source and site operation software that lets clinical research organizations streamline their efforts. With this solution, you and your team can create and customize pre-made templates from the built-in library, thereby saving you time and letting you focus on critical matters.

Specifications

  Business Size
Small, Mid-Market, Enterprise
  Deployments
Premise
  Language Support
English
  Platforms

Product Details

Features

Enrollment Management

Document Management

Monitoring

Recruiting Management

Study Planning

21 CFR Part 11 Compliance

Electronic Data Capture

HIPAA Compliant

Patient Database

Scheduling

PDF Annotation & Electronic Signature

Event Creation

One-Click Call & Text

Payments Reconciliation

Budget Configuration

Benefits

Time-Saving Solution

With Clinical Research IO, you can look forward to more time doing clinical trials and other critical aspects of the workflow. The solution helps you reduce the time spent on filling up and filing papers with its automation capabilities. Thus, it helps you minimize manual work and lessen the possibilities of re-work.

Quality Enhancement

Clinical Research IO can aid you in improving the quality of your trials’ data. It helps you decrease deviations and abstract sticky notes from your processes. Other than that, the software provides you with 100% real-time and accurate information through its reporting suite as well as a single source of truth between your electronic data sources and CTMS.

Improved Recruiting

You can use Clinical Research IO to improve your subject recruitment. The software has an integrated one-click call and text module that helps you instantly communicate with your prospects. You can keep track of your exchanges with them right within their profiles so you can rest assured that your subject data are well organized.

Remote Site Management

Clinical trials do not happen at single sites and that is something the people of CRIO understand. That is why the Clinical Research IO helps you standardize your workflows to reduce oversights. And in case errors occur, you can immediately act on them because of the centralized system.

Anywhere Clinical Data

Clinical Research IO frees you from paperwork and aids you in going mobile with your data. The solution is a cloud-based one and allows you to access clinical trial information even when you are out of town so you can keep a pulse on progresses.

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