NONCLINICAL OPERATIONS SUPPORT
TOXPLUS Monitoring is a dedicated, client-focused company that provides global nonclinical operations support services. We provide qualified, experienced nonclinical study monitors, vendor auditors, and study managers for studies conducted under Good Laboratory Practices (GLP) as well as studies not conducted under GLP. We serve pharmaceutical and biotech companies with early and late stage drug development programs.
TOXPLUS Monitoring IS YOUR NONCLINICAL STUDY MONITORING PARTNER
Nonclinical study monitoring is essential to ensure a study for drug development is conducted ethically. The company that sponsors a study for drug development is responsible for such oversite.
Our study monitors ensure that a study is conducted in compliance with an approved protocol, protocol amendments and regulatory guidelines. They provide oversite of proper data collection and documentation of study results.
DEDICATED AND KNOWLEDGABLE PROFESSIONALS
Our Team has decades of experience working with contract research organizations (CROs), in industry and in consulting.
If you need support for your upcoming study or program, contact TOXPLUS Monitoring at [email protected] or schedule your Study Monitor here.
