Articles
RELIABLE DATA FOR INFORMED DECISIONS: Non-clinical & Bioanalysis Services for safety pharmacology
At Biotrial, we recognize the essential role of safety pharmacology in advancing drug
development with confidence. Our non-clinical services are designed to support the specific
needs of each program, providing scientific expertise, operational flexibility, and robust in vivo
capabilities across multiple species, with animal welfare at the heart of our approach.
From early discovery to regulatory development, our teams generate high-quality non-clinical
data to assess safety, characterize pharmacological effects, and guide decision-making. This
expertise is complemented by our state-of-the-art bioanalytical laboratory, which provides
reliable analytical support to strengthen and interpret non-clinical study outcomes.
OUR PRIORITIES
Our priorities are focused on delivering accurate, reliable and defensible data to support confident decision-making.
We are commited to providing high-quality results in a timely manner, while developing robust, reproducible and translational models and methods, designed to generate meaningful outcomes and ensure scientific rigor, consistency and relevance.
WHAT MAKES US DIFFERENT
As a one-stop shop CRO, Biotrial combines a global experience with specialized scientific expertise to support our clients throughout every stage of development.
With our 2.500m² / 27.000 sq ft of non-clinical laboratories on site, we offer highly customizable solutions designed to provide the flexibility and adaptability required for each project.
Our teams develop innovative models and apply a translational approach, supported by customized LC-MS/MS methods with pg/ml sensitivity.
Finally, rapid start-up, flexible project execution and dedicated scientific support allow us to work as a true scientific partner, helping innovation and discoveries move forward efficently and confidently.
OUR
NON-CLINICAL
SERVICES
- Efficacy Pharmacology studies
- Safety Pharmacology studies: early derisking studies and GLP IND regulatory studies
- PK/PD studies: pharmacokinetics (compartemental & non-compartemental) and pharmacodynamics
- Model development at the sponsor’s request
OUR BIOANALYTICAL SERVICES
- Method development, validation & production
- Extensive expertise with the LC-MS/MS system
- GLP non-clinical sample analysis
- Common & Explicit human/animal matrices
- Molecule and metabolite quantification
- Quantification ranging from ng/mL to pg/mL sensitivity
To learn more about our services, contact us at contac@biotrial.com
