At QPS, we have systems in place to enable the identification, recording, reporting and analysis of safety information so that any safety signals that arise during a trial are quickly identified and acted upon.
Our safety reporting and pharmacovigilance services include:
- Creation of safety management plans.
- Development of your safety database.
- Safety reporting both electronically and on paper.
- Maintenance of safety databases for your studies.
- Medical Monitoring
- Complete safety management of your clinical study including medical review.