Our internal Quality Assurance Team ensures that clinical trials are
conducted per protocol and within ICH/GCP guidelines:

> QA services performed by former big pharma monitors

> Regulatory Affairs Advisor has 37 years of experience with the US Food and Drug
    Administration

> Comprehensive SOPs and employee training records

> Strong foundation in ICH/GCP/CFR highlighted by over 75 sponsor and agency audits     without significant findings or 483s issued