The mission of a QA department is to ensure clinical data accuracy and integrity through a systematic and independent examination of all trial-related activities and documents.

Our aim is to achieve the highest performance in clinical trials by maintaining a continual review of consistency and documentary evidence of quality throughout the clinical development process. 

CROS NT’s internal system audits, vendor audits and structured training programs enables us to avoid risks and eliminate systematic problems. The quality management system ensures that data is recorded, analyzed and accurately reported according to Standard Operating Procedures (SOPs), ICH/GCP guidelines and FDA requirements.

CROS NT is also 21 CFR Part 11 compliant and ISO 9001:2008 certified.