Currently the following services are provided by IPR-EE and its clinical
sites:
- Project management
- Writing protocols and CRFs and ICFs in English and Russian
- Comments on protocols and CRFs and translation of documents
- Preparing of source data books in Russian
- Submitting EC vote, approval at authorities, import-, export
- licences
- Patient/volunteer recruitment
- Clinical phase in own clinical sites
- Quality control of trial documents and quality control during clinical
- phase
In collaboration with experienced partners IPR-EE can offer additional
services:
- Bioanalytics of samples
- Pharmacokinetics
- Data management
- Statistics
- Report writing
- Registration of compound in the EU
- Marketing Support