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Clinical
Data Solutions
InForm™
GTM: Global Trial Management
Phase Forward’s InForm Global Trial
Management (GTM) system delivers advanced EDC functionality
in an award- winning solution that has already been used successfully
in over 3,100 trials.
Clintrial™:
Clinical Data Management
The Clintrial product offers a comprehensive,
regulatory compliant clinical data management system used to
collect, manage and review clinical data.
WebSDM™:
Applied Data Standards
The Web Submission Data Manager application
allows users to load SDTM-format study data, check and correct
errors and browse data in a variety of tabular and graphical
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Global
Trial Supply Management
Phase Forward
IRT Solution
Phase Forward's IRT solution
provides a next generation, fully Web-integrated Interactive
Response Technology (IRT) to help streamline clinical trial
randomization and trial supplies management activities. |
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Phase
I Clinic Automation
LabPas™
Phase Forward’s LabPas software product
suite allows users to automate and integrate key Phase I clinic
processes. |
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Safety
Solutions
Phase Forward’s innovative Empirica
suite was designed to help companies manage pharmacovigilance
activities strategically.
Empirica™ Study: Clinical Trials Signal Detection
Empirica™ Signal: Strategic Pharmacovigilance
Empirica™ Trace: Adverse Event Reporting
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Data
Analysis and Report Management
Waban™ SCE
Waban™ Statistical Computing Environment
(SCE) provides process and workflow capabilities to securely
manage vital statistical programs and help organizations control
and validate the clinical data sources and routines used for
any analysis.
Waban™ CDR
Waban™ Clinical Data Repository (CDR) provides
a data repository for storing and managing clinical trials data
(including metadata).
Waban™ LIMS
Waban™ Laboratory Information Management
System (LIMS) supports clinical genotyping, sequencing, expression,
microarrays, affymetrix, pre-clinical, clinical pathology, and
other pharmacogenomics and biomarkers related processes.
Waban™ SMS
Waban™ Specimen Management System (SMS)
is a comprehensive system designed to meet the complex workflows
and processes involved in handling, receiving, shipping, and
storing of samples collected for use in clinical trials and
for biobanking. |
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Late Phase and ePRO Solutions
OutcomeLogix™ Site Reported Data Capture
OutcomeLogix™ Reported Data Capture provides sites the ability to collect clinical data via a web-based interface. OutcomeLogix walks the user step-by-step and form-to-form through the data collection process.
OutcomeLogix™ ePRO
OutcomeLogix™ ePRO provides an intuitive interaction to support patient reported or third party reported observational data collection via a web-based or handheld interface.
SleepLogix™
SleepLogix™ is designed to be a graphical illustration of the values and time points directly entered by patients. SleepLogix is a customized tool that has been created for use in clinical trials and observational applications as well as in general use in sleep clinics.
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