CIRION is a knowledge-based, GLP-compliant Central Laboratory dedicated to providing project management services and scientific expertise for Phase I to IV clinical studies.
CIRION has developed expertise in the management of complex clinical research projects. Whether your project includes investigative sites around the world or involves specialized testing, CIRION delivers results within your timelines.
Full Service Central Laboratory with Global Reach
- North America (Canada and USA)
- Central and Eastern Europe
- South America (Argentina and Brazil)
- Australia and New Zealand
- Asia (Singapore and Taiwan)
CIRION has developed a network of CAP-accredited central laboratories across the world to assist in the regional support of investigative sites and the analysis of fresh biological specimens during the course of your global clinical projects.
CIRION oversees all interactions with the partner laboratories and ensures logistical activities run smoothly. All data can be integrated into a single database. We remain the point of contact throughout the project so that all of these interactions are seamless to you.
All testing is performed according to specifications defined and quality assured. To ensure the integrity of your data, regular quality control proficiency testing and cross-validation or correlation of equipment are performed between laboratories to ensure there are no significant variations between results and reference values.
Our QA unit qualifies our partner laboratories to adhere to strict standards as well as CIRION Standard Operating Procedures (SOPs) to ensure the highest level of quality expected at CIRION is provided by our partner laboratories. The CIRION QA unit will also audit key study documents such as the clinical protocol, laboratory manual, EDT Transfer agreement, and the multisite workplan which will outline the key responsibilities of each partner in your clinical study.