Trialwise
Quality assurance and auditing, medical monitoring and clinical development services.
What they do
From their website
Augmented services
Data management
Clinical operations
- Site/Investigator Identification and Qualification (opens in a new tab)
- Central IRB Submissions (opens in a new tab)
- Study Monitoring (opens in a new tab)
- Investigational Product Management (opens in a new tab)
- Trial Master File Management (opens in a new tab)
- Study Specific Plan Development (opens in a new tab)
- ICF Development (opens in a new tab)
- Source Document Development (opens in a new tab)
- Vendor Management (opens in a new tab)
- Risk Identification and Management (opens in a new tab)
Show all (44)
Medical writing
- CSR Addendum Documents (opens in a new tab)
- Electronic Publishing (opens in a new tab)
- Investigator Brochures (opens in a new tab)
- IND Support (opens in a new tab)
- Trial Registration and Results Disclosure (opens in a new tab)
- Protocols and Protocol Amendments (opens in a new tab)
- ADME (opens in a new tab)
- First in Human (SAD and MAD) (opens in a new tab)
- Drug-Drug Interaction (opens in a new tab)
- Thorough QTc (TQT) (opens in a new tab)