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Clinical Research Support
- Preparing Clinical Trials
- Study design consulting
- Determining treatment group sizes
- Preparing statistical sections of
study protocols
- Randomization
- Support with design of study
documents
- Data Management with OpenClinica
(compliant with 21CFR Part 11)
- eCRF
- Coding (MedDRA, WHO)
- Statistical Analysis (SAS) of Clinical
Trials in accordance with GCP principles
- Final Study Reports
- Publications
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