SyMetric BIO

Bio-availability and Bio-equivalence (BA/BE) studies are characterized by the duration, subjects/volunteers involved, types of visits, administration of the investigational products and the pace of procedures conducted during the study. Standard IRT/IWRS and EDC products used for clinical end-point studies cannot handle the BA/BE studies.


SyMetric BIO is a cloud based web platform exclusively built to handle Bio-availability and Bio-equivalence (BA/BE) studies. The specialized features of this product can easily handle short duration, open label, multi-arm, cross over studies over any number of periods. In addition; the full-fledged project management features of CTMS, data management features of EDC, Medical Coding, and Pharmacovigilance functionalities are bundled into this platform.

SyMetric BIO is completely 21 CRF Part 11 and ICH - GCP compliant. It is designed exclusively to drive the business processes which are specific to BA/BE studies such as check in and check out, ambulatory visits, monitoring washout periods etc. With a wide range of inbuilt data management functionalities such as Discrepancy handling, Source Data Verification, CDISC/SDTM data exports, medical coding, AE/SAE reporting, bookmarks it eliminates the need for having multiple systems to perform each function.

Volunteer Management System

Perform fool proof volunteer registrations using Biometric-aided enrollments

Interactive Response Technology

Parallel or Crossover based Treatment assignment to Subjects

Laboratory Management System

Effectively manage and integrate lab data into the eCRF to improve lab efficiency

Electronic Data Capture

Capture clinical data of Subjects into streamlined and simplified eCRFs

Sample Management System

Track samples as they make their way through the scientific processes in a study

Clinical Trial Management System

Track and monitor the progress of an individual or multiple projects

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Advantages

HIGHEST LEVEL OF DATA QUALITY
MINIMAL IT VENDORS MANAGEMENT
SIGNIFICANT REDUCTION IN RESOURCES
SHRUNKEN PROJECT TIMELINES
FASTER STUDY DATA SUBMISSIONS
LOWEST TCO
Quick Setup
User Friendliness
Compliant to Industry Standards
Well defined SOPs & Quality Policy
Context sensitive Help Documentation
Built in Ticketing System
User accountability through audit trails
Configurable Messages
Completely Integrated on Single Database
One-Stop-Shop
Real time data in Reports/Dashboards
Transparent and Simple Pricing