• 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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