Eolus combines extensive knowledge of clinical requirements and deep experience with clinical processes to help you efficiently plan, manage, and execute your clinical trials. Our goals is to enable you accelerate the time from research to market.
- Clinical site evaluation, qualification and selection
- Data design, review, development and management
- Electronic Data Capture
- Database and process audits
- Clinical procedures development
- Good Clinical Practices (cGCP) audits and training
- Source data reviews
- FDA Inspection Preparation
- IVRS/IWRS Selection and Review
- Study Management and coordination
- Electronic Trial Master File (eTMF) Reviews
- Pharmacovigilance (PV)
- Adverse Events (AE)
- Serious Adverse Events (SAE)