BioClinAarc provides end to end (e2e) comprehensive clinical data management solutions from Data Management Plan to Database Lock. Our expert clinical data management services are designed to make every part of the clinical research data management process better organized and more foreseeable. As a result, biopharmaceutical companies recognize the value of high quality data, delivered in a cost effective manner.
Clinical Data Management services includes:
Project Management
On-shore & off-shore CDM Services
Data Management Plan (DMP) development
CRF/eCRF design and development
CRF Completion Procedures
CRF Annotation & Review
Database Build & Design
Data validation specifications
Edit checks Programming & Testing
Data processing through double data entry
Query Management
Medical Coding
Safety Data Management & Reconciliation
Laboratory/Vendor Data Reconciliation
Data Export/Transfer
CDASH Compliant deliverables
Key features:
SAS Suite PheedIt
SAS Analytics
21 CFR Part 11 compliant systems
ISO 27001:2005 certified for Information Security Management System (ISMS)
30 employees with 5-10 years of domain expertise
Electronic data capture (EDC) platform encompassing 40 countries
Extensive capability in sponsor hosted technologies
This section of our website will enable you to learn more about becoming an BioClinAarc Investigator and also provides a dedicated resource centre for Investigators working with BioClinAarc Central Laboratories.
