Clinical Trial Design
Advice on the design and conduct of clinical trials
Protocol review
Data Centre
Data Capture (electronic and paper based case report form)
Interactive Voice Response System and randomisation
Web portals facilitating e-trials
Data Management
Clinical event and drug coding
Biostatistics
Additional Resources
Study Initiation
Sponsor, ethics & regulatory approval
Other Services
Consultancy
Health Economics
Endpoint Committee co-ordination
IDMC Reporting and co-ordination
Training
Study Conduct
Clinical Services
Trial Management
Monitoring
Pharmacovigilance
