- Statistical analysis focused on clinical studies in all phases (I, II, III, and IV).
- Design of CRFs, review, and guidance for their implementation.
- Specialized medical coding (WHO and MedDRA).
- Proposal and SAS programming for EDIT CHECKS for plausibility (QUERIES).
- Sample size calculation.
- Biostatistical analysis (SAS).
- Integration of medical-statistical report according to ICH.
- Medical writing.
Contamos Con
Contamos Con
Contamos Con
Temperature and humidity monitoring that guarantee good storage practices for the product under investigation.