Clinical Trials
End-to-end support for clinical trials, from planning and start-up through monitoring, quality control and close-out.
What we provide
11 services, available individually or as one engagement.
- 01
Clinical trial planning and study start-up
- 02
Protocol and study document development and review
- 03
Site selection and site readiness
- 04
Regulatory and ethics submission support
- 05
Investigator and study-team training
- 06
Clinical trial monitoring and site support
- 07
Study coordination and quality control
- 08
Source data and essential document review
- 09
Data quality and clinical research documentation
- 10
Protocol deviation and compliance support
- 11
Close-out and study reporting
Who this is for
- Pharmaceutical and biotechnology sponsors
- Contract research organisations (CROs)
- Research institutions
- Universities
- Investigators and research sites
- Academic trial units
Related training
- Clinical Trials & Good Clinical Practice (GCP)
- Research Ethics & Good Research Practice
- Data Collection, Management & Analysis
Talk to us about clinical trials
Tell us about your study, evaluation or training need. We will reply with how we can help and who on our team would lead it.