What is Clinical Data Management?
Every clinical trial run by a pharmaceutical company, biotech firm or CRO generates large volumes of patient data. CDM professionals collect, enter, validate, clean and prepare that data for statistical analysis and regulatory submission.
In short: CDM makes trial data accurate, reliable and ready for analysis.
Database Design & Development
eCRFs, data collection systems and protocol-driven database configuration.
Data Entry & Management
Accurate entry, patient record review and complete study records.
Data Validation & Cleaning
Edit checks, discrepancy detection, and raising and resolving queries.
Data Review & Quality Control
Dataset review and QC checks in line with protocol, GCP and regulations.
Database Lock & Study Closure
Final cleaning, reconciliation and query closure ready for analysis.
Data Standards & Programming
CDISC standards, SDTM and ADaM datasets, transformation and validation.
Who we will serve
Pharma & Biotech
Manufacturers and sponsors running clinical trials who need outsourced CDM support.
CROs
Domestic and international, small and mid-sized CROs outsourcing CDM workloads.
Global Capability Centres
Supporting GCC clinical data operations — and exploring a new GCC through our network.
