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Target Health

Name: Target Health
Rating: 4.5 (2 reviews)

By Target Health

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Highlights : About Target Health

Document Management

Patient Database

21 CFR Part 11 Compliance

Enrollment Management

Electronic Data Capture

Study Planning

About Target Health

Target Health Software Suite is a full-service medical research platform designed to help organizations accomplish paperless clinical trial requirements. Aside from the system’s primary eSource electronic data capture (EDC) software, the cloud-hosted platform includes a clinical trial management system (CTMS), digital Informed Consent, electronic patient reported outcomes, and results-based reports. All these are beneficial for biopharma companies, medical device sposors, academic medical centers, and contract research organizations (CROs).

Specifications

Business Size

Small, Enterprise

Customization

Yes

Deployments

Cloud

Language Support

English

Platforms

Product Details

Features

Study Planning

Patient Database

Monitoring

Document Management

Scheduling

21 CFR Part 11 Compliance

Enrollment Management

Electronic Data Capture

Benefits

Target Document® is a secure, easy-to-use, cloud-hosted document distribution and management system which allows users to post, share, electronically sign, search, and archive any electronic document.

Target Encoder® is a safe and intuitive web-based coding tool used for CRF terms, to MedDRA, and WHODRUG. Upon the inputting of CRF terms into the System, each is searched in the designated MedDRA or WHODRUG database.

The Target e*CTR™ clinical trial record system provides regulated document management system that is fully integrated with Target e*Studio and all the other components of the Target Health eSource’s platform. This feature safekeeps all eInformed Consent form, SAE form, and all the other pertinent files. Version control is also available.

Target Health Software Suite’s solutions include Target e*ICF®. The electronic Informed Consent form enables study subjects or legal representatives to review the informed consent form from the web. Users may also inquire about the study and electronically sign the ICF in any language.

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