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Clinical Trials

Data Management

ClinTec provides a full-service solution for Clinical Data Management and Biostatistics ensuring the delivery of high quality clinical trial data in the most cost effective way for your project.

Our Data Management specialists have many years of experience within different therapeutic areas and of managing both EDC and paper studies. Supported by the appropriate CDMS systems they ensure that your database lock is timely without sacrificing data quality

Our services in Data Management

Data Management input during protocol development

CRF design

Database design and validation

Electronic exception check programming and validation

Data Collection: Electronic Data Capture (EDC) or manual Data Entry from paper CRFs

Data handling and data cleaning in our 21 CFR part 11 compliant CDMS, according to ICH-GCP

Ongoing QC of data including final QC prior to Database lock

Coding of medical terms (Medications, Secondary Diagnoses and Adverse Events) according to MedDRA

Ongoing Serious Adverse Event Reconciliation

Integration of third party vendor data including ECG data, Central and local laboratory data, imaging data and PK data

Transfer of high quality data for statistical analysis and submission to the regulatory authorities, according to CDISC or client specific data standards

Data Management consulting/training for implementation of new systems, coding & dictionary management or creation of new Standard Operating Procedures (SOPs)