Safety Coverage Provided by Qualified Physicians
Throughout the clinical development and post-marketing phases, our qualified medical professionals and extensive network of specialists can provide a range of quality services to meet your needs.
We offer 24/7 medical monitoring by qualified physicians to ensure participants’ safety in clinical trials. Our qualified physicians can provide:
- Protocol clarifications
- Pharmacovigilance
- Global serious adverse events (SAEs) monitoring and case narrative preparation
- Clinical/safety medical management
In addition, our MDs work collaboratively with our competent medical writing team to deliver the safety documentation for your study or clinical trial. Our service offerings include:
- Clinical study protocol development and review
- Subject eligibility evaluation
- Informed consent form development and review
- Serious adverse events (SAEs) reporting
- Benefit and risk assessments
- Medical coding of safety events
- Safety database