Clinical Data Management
Accovion provides full data management services for all types of studies – medicinal products and drugs, medical devices, from routine phase I trials through to large and complex phase III trials, as well as non-interventional studies.
Our experienced Data Management team ensures that the clinical data in your project is collected and managed reliably, efficiently and in compliance with industry standards and regulatory requirements. Accovion Data Management services offer maximum flexibility for conducting clinical trials with EDC, paper CRFs or a combination of both, on our systems or yours.
We have many years of experience working with our own fully validated clinical data management system – Oracle Clinical® - as well as working on our clients’ systems and other EDC vendors.
Experience & Expertise:
- CRF design
- Database design and programming
- Programming of edit checks and data listings for data validation
- Coding of diseases, adverse events and medications
- Query management
- Standardized and customized status reports
- Support for medical review and SAE reconciliation
- Integration of data from other sources
- Patient reported data
- Help Desk
- (e.g. CDISC, regulatory requirements)
- Work according to Accovion or Client standards and processes
Director Clinical Data Management
+49 6196 7709-433