Clinical Data Management
CLINICAL DATA MANAGEMENT
We are committed to supporting your company from the design of the clinical trial to study closure, and ensuring the highest level of data quality. We offer robust systems that meet regulatory guidelines (FDA, EMA) and conventions, including 21 CFR Part 11 and ICH-GCP. Let the experts at Crescentyards guide your company through the entire data management lifecycle.
Our data managers work to ensure on-time results of your clinical trial data. Crescentyards delivers your data before critical deadlines. While we offer quick turnaround times, we never sacrifice the quality of our results.
From clinical development planning to data delivery, Crescentyards is committed to customizing data management solutions that emphasize accuracy, integrity, accountability, and transparency as much as agile reporting. We take pride in producing results that are reproducible, source-verified, delivered on time, and cost-efficient.
Our Services Include:
(e)CRF design and preparation of annotated CRF
Third party vendor management
Database design
Clinical data entry
Preparation of statistical or integrated reports
Laboratory data handling
Medical/Dictionary coding
SAE reconciliation
Setting up status reports and statistics
Knowledge and use of current data standards (SDTM, CDASH, and other CDISC standards)
Quality control and data base lock
(Blinded) Data Review
Data validation and query management
Our Services Include:
(e)CRF design and preparation of annotated CRF
Third party vendor management
Database design
Clinical data entry
Preparation of statistical or integrated reports
Laboratory data handling
Medical/Dictionary coding
SAE reconciliation
Setting up status reports and statistics
Knowledge and use of current data standards (SDTM, CDASH, and other CDISC standards)
Quality control and data base lock
(Blinded) Data Review
Data validation and query management