Welcome to Booth 825! We look forward to meeting you!
TOXPLUS Monitoring is a dedicated, client-focused company that provides global nonclinical study monitoring services, non-GLP and GLP vendor qualifications and study management services.
We provide qualified, experienced study monitors oversee critcal aspects of your study conduct. We serve pharmaceutical and biotech companies with early and late stage drug development programs.
Vendor qualification audits are important for both GLP and non-GLP studies and are a Sponsor’s responsibility for due diligence. Although not ideal, these can also occur shortly after study placement or study start. TOXPLUS Monitoring provides vendor qualification audit services of preclinical CROs to support your drug development program.
Our study management services are tailored to meet your specific needs. TOXPLUS Monitoring can serve as Sponsor representation, including protocol review and ensuring that the study is executed per protocol, as well as regular updates with the Sponsor and Study Director.
Contact us to meet at ACT: alynch@toxplusmonitoring.com OR kanderson@toxplusmonitoring.com
Brands: TOXPLUS Monitoring