Because quality and attention to detail are paramount for translating research into life-saving innovation, Surpass is committed to excellence in all that we do.
Our comprehensive Quality System addresses all necessary requirements and is maintained by our regulatory compliance/quality assurance team. By staying active in industry groups such as the Society of Quality Assurance (SQA), our team keeps abreast of recent regulatory trends and actively updates our systems to address current requirements.
Make Surpass your trusted preclinical CRO partner. Contact us today.
Our professionals have extensive experience conducting GLP studies for regulatory submissions or internal review board (IRB) applications. Check out our GLP Studies page for more details.
Because Life Depends On It.