Orbis Clinical provides dedicated consultants within drug safety, pharmacovigilance and risk management to augment existing teams, outsource spikes in workload, or to bring an added level of subject matter expertise to your organization.
- Case processing, Data entry, triaging, coding, narrative writing for clinical and post marketing
- Medical coding/MedDRA, WHO Drug
- Scientific Literature Review
Physician level support
- Medical Case Review
- Aggregate Data Review
- Risk Mgmt. Development
- Safety Signal Detection
- Submission Writing
- Database SMEs (Clintrace, Argus, ARISg, RAVE)
- PV Compliance & quality assurance
- PV Auditing
To learn more about our services, contact us today!