EDC System for Clinical Trials

Digitize clinical trial processes to become more productive with 123 Form Builder. Deliver life-saving drugs to those who need them most. All while maintaining security and compliance.

EDC System for Clinical Trials

Our clients

Easy to manage digital forms to help with your clinical trial

Easy to manage digital forms to help with your clinical trial

Easy to manage digital forms to help with your clinical trial

  • Deliver better drugs, at lower costs
  • Help participants enroll in clinical trials easier
  • Stay compliant and secure
  • Eliminate inefficient document workflows

Better electronic data capture, faster drugs discovery

Better electronic data capture, faster drugs discovery

Better electronic data capture, faster drugs discovery

Say good-bye to wasting time with paper forms. With 123 Form Builder you can transform the manual way research teams design clinical trials into seamless workflows that automatically send data to other systems your organization uses. This is how you get to improve the speed and efficiency of innovative clinical trials.

Benefits

  • Workflow automation for clinical trial operation
  • Create, sign and store documents digitally
  • Stay GDPR and HIPAA compliant every step of the way
  • Streamline patient scheduling, preauthorization and preapproval prior to patient visits and procedures
  • Complete clinical report studies, consent online, including HIPAA authorization, procedure consent, program enrollment, and more
  • Pull data from multiple external systems of record to provide a single view of patient information

Data capture automation for clinical trials

Data capture automation for clinical trials

Data capture automation for clinical trials

Automation impacts care delivery and operational efficiency. With 123 Form Builder, you can start securely optimizing and automating critical clinical and business workflows, and rely on complex conditional logic, multi-page and multilingual forms, Salesforce integration, and Zapier & API integration.

Areas where automated processes make clinical trials more efficient:

  • Case report form development

    Data gathered during clinical trials by way of case report forms (CRFs or eCRFs).

  • Clinical metadata management

    Centralized systems that allow you to store and manage your metadata assets such as forms, datasets, edit checks, and controlled terminologies.

  • Dataset conversion processes

    During the phases of a clinical trial, data must be submitted and resubmitted in the correct CDISC format to the FDA many times for review.

Minimize risk exposure in clinical trial data collection

Minimize risk exposure in clinical trial data collection
  • Features
  • GDPR compliance
  • US/EU storage of data
  • HIPAA Compliance
  • Custom contract
  • Advanced security and privacy control

Minimize risk exposure for clinical trial data

We know your research still depends on legacy software products, spreadsheets, and paper-based tools to maintain critical healthcare equipment.
Siloed processes and manual workflows make it harder to keep clinical trials secure and compliant

But now, you can collect data for clinical trials with confidence, knowing you’re doing so in a secure and compliant manner. With 123 Form Builder, you minimize risk exposure for clinical trial data collection, and help your organization move forward, faster. No more managing different regulations in different countries – focus on what’s important to you.