Our Services
IRMS is fully equipped to offer a wide range of Clinical Research Services to its clients. We comply with GCP, GLP and other applicable regulatory and statutory requirements to meet the criteria of Quality, Data Integrity, Safety and Ethics.
The array of our service capabilities include:
SMO - Site Management Organisation
- Project Management
- Site Management
- Clinical Trial (Phase I-IV)
- Early Phase Studies (BA/BE,PK/PD)
Medical Writing
- Manuscript
- CSR (Clinical Study Report)
- Protocol Development
CDM
- Clinical Data Management
Statistical-Analysis
- Bio Analysis
- Pharmacokinetics & Pharmacodynamics
- Bio-Statistical Analysis