Clinical Data Management — IDDCR Global Research
Clinical Data Management
Robust data collection, validation and integrity across the clinical data lifecycle.
IDDCR delivers end-to-end clinical data management services — from CRF design and database build through data cleaning, reconciliation and database lock — ensuring submission-ready data of the highest quality.
Our Approach to Clinical Data Management
Our clinical data management team combines deep domain expertise with modern EDC platforms and data science capabilities to deliver clean, accurate and audit-ready clinical trial data. We apply rigorous data review processes, automated validation checks and proactive query management to maintain data integrity throughout the study lifecycle.
Core Capabilities
CRF Design & Database Build
Electronic CRF design, annotated CRF development, database build and UAT in leading EDC platforms including Medidata Rave, Oracle InForm, REDCap and Veeva Vault.
Data Validation & Edit Checks
Comprehensive edit check programming, validation rule development and automated data review to identify and resolve data discrepancies in real time.
Query Management
Systematic query generation, tracking and resolution with sites, ensuring timely data cleaning and minimising outstanding queries at database lock.
Medical Coding
Accurate medical coding using MedDRA and WHO Drug dictionaries, with coding conventions aligned to sponsor standards and regulatory requirements.
Data Reconciliation
SAE reconciliation, laboratory data reconciliation, PK data reconciliation and external data vendor management to ensure data completeness and consistency.
Database Lock & Transfer
Formal database lock procedures, data transfer to biostatistics, audit trail review and archiving in compliance with 21 CFR Part 11 and ICH E6(R2).
Therapeutic Areas
Development Phases
Explore Other CRO Services
Frequently Asked Questions
Common questions about this service — answered by our specialist team.
Need Clinical Data Management Support?
Speak with our CDM team about your study requirements and how we can deliver clean, submission-ready data.