Superior processes from start to finish
MetaPharm Inc. offers full clinical data management services for Phase I-IV clinical trials and non-interventional/post-authorization studies. We draw on experience in various therapeutic areas gained through complex long-term projects, allowing us to create reliable timelines and ensure timely delivery of data.
Our committed team has worked together for over 12 years. Clinical data management, clinical operations and our statistics teams work hand in hand to identify, mitigate and monitor risks throughout the project.
Our ability to construct studies on several EDC platforms allows us to offer the best fitting tools tailored to your specific project while maintaining full oversight throughout the study. To find out how we can support all your clinical data management needs, simply contact us.
We possess the expertise, know-how and tools to efficiently manage your study and beat timelines.
- CRF design
- Electronic data capture setup
- Data management plan
- Clinical database setup
- Data validation plan
- Data review, reconciliation and cleaning
- Data transfer specifications and data integration
- Team trainings
- Double-data entry
- Data quality control
- Status reporting
- Ad-hoc reports
- Centralized evaluations, e.g. central-diary evaluation and clinical outcomes assessment evaluation
- Randomization and custom IMP logistic workflows
- Database lock
- Scanning and bookmarking
- Archiving deliverables
- Clinical trial result posting in EudraCT