Benchmark against your competition
Understand how AI crawlers access your site
See where AI gets info about you
Track the queries mentioning your brand
Own your AI narrative
Add GEO to your service offerings
Get recommended in shopping queries
Monitor AI mentions at scale
QPS is a GLP/GCP-compliant contract research organization (CRO) founded in 1995, providing comprehensive preclinical and clinical research services to pharmaceutical and biotechnology clients worldwide. With over 25 years of experience, QPS offers custom-built solutions in drug development, ensuring high-quality deliverables and efficient project management.
Claim this profile to keep your information accurate and add what's missing.
Includes pharmacology, toxicology, DMPK labs, bioanalysis, and translational medicine to support pharmaceutical development.
Full-service clinical development from first-in-human trials through Phase IV, offering comprehensive support for clinical research.
Global regulatory affairs solutions designed to ensure effective asset development and stakeholder management.
Custom-built medical affairs solutions to support efficient and effective product development.
Expert safety reporting services to safeguard patients and support sponsors.
QPS conducts a wide range of preclinical and clinical studies, including pharmacology, toxicology, DMPK, and various clinical trial phases.
QPS's DMPK work is conducted in labs located in Newark, Delaware, USA.
QPS is committed to delivering outstanding quality by meticulously managing every aspect of studies and ensuring high-quality deliverables.
QPS has over 1,250 employees with extensive experience in drug development, supported by a senior leadership team with several hundred years of combined industry experience.
QPS focuses on bioanalytics and clinical trials, creating value for patients and clients while fostering employee growth.