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Excellent planning and resources can ensure that your studies yield high quality data within strict timelines and budget requirements. Our Data Management service has years of experience in providing a full range of data management services for the pharmaceutical, biotechnology and medical device industries, across many therapeutic areas. We have the experience, capacity and technological innovation to meet today's pressures in speeding processes to database lock while retaining high quality deliverables. Ultimately, we help our clients make important decisions at the earliest. Our data management services are tailored to fit your clinical trial needs and our SOPs can address paper-based, fax-based, and EDC-based systems so that each Sponsor's project specifications can be accommodated.

Services
Case Report Form (CRF) Design
Clinical Data Management Plan
Database Design
Validation Rules
Double Data Entry
Electronic Data Capture (EDC)
Handling External Data
Query Management
Dictionary Services (MedDra, WHODD or your own dictionary)
Quality Control
Serious Adverse Event Reconciliation
Data Listings
Database Lock
 
 
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