Preclinical Cardiovascular Expert
Preclinical Expertise
A preclinical CRO expert in cardiovascular pharmacology and electrophysiology
PhysioStim is a discovery and preclinical CRO expert in pharmacology and electrophysiology on cardiovascular and vascular functions over two decades. We study the effects of compounds (and biologics), whatever their therapeutic areas for various purposes: mandatory safety, secondary pharmacology or toxicology study.
We offers a wide selection of ion channel assays as well as additional cardiac safety studies in compliance with all ICH S7A and S7B guidelines and Good Laboratory Practices. We are a preclinical Contract Research Organization of highly experienced cardiovascular pharmacology and electrophysiology experts. As preclinical cardiovascular expert, PhysioStim provide a wide range of possibilities to conduct both your mandatory and complementary ion channel assays for reliable and efficient cardiac safety studies. We also respect the 3R principle and have already taken steps to comply with the upcoming CIPA guidelines.
THE RIGHT TEAM TO OPTIMIZE YOUR R&D LEAD TIME
As preclinical cardiovascular expert, we are very attentive to trends in pharmaceutical companies such as the outsourcing of non-clinical studies and the need to be close to CRO study directors. We also able to adapt our standard and perform customized studies to pefect meet our client’s needs. We bring out the cardiovascular aspects at the earliest during drug discovery phases to be efficient in drug development. We provide advanced models for cardiac safety studies to help pharmaceutical and biotech companies reduce the R&D lead time of their drug by:
- Studying the safety of compounds during preclinical trials
- Derisking compounds at an early stage
- Helping them select lead candidates during the preclinical stage
- Determining compounds able to induce QT prolongation
High quality preclinical cardiovascular electrophysiology studies
- Close relationship with your study director, who keeps you up to date at every stage of the study
- Expert advice to help your project move forward
- Continuous in-house training of all our staff members (GLP, multisite studies, new technologies…)
- Tracability of all study data
- All raw data are audited by our Quality Assurance Department
- Guaranteed confidentiality
- Quality at every phase of your study, even in non-GLP studies
- High quality GLP-certified data in a GLP-certified environment, even in screening studies
- Compliance with ICH S7A and S7B guidelines
- Respected deadlines
