SOP and internal processes development to ensure consistency across programs.
Provision of trained Study Coordinators.
Grant payment guidance (based on market data).
- PMRs (Plan de manejo de riesgos)
- Study Clinical Documents
- CSR (Clinical study report).
Study feasibility and Site Selection.
SAP (Statistical analysis plan)
Study Start up and Regulatory Services.
Monitoring - Phase 1 to Phase 4 studies.
Import and export services.
Outsourcing of specialized staff.
Consultancy on LA Clinical Research Processes.
Matías Romero 102, Int. 205
Del Valle, Ciudad de México, 03100México
Mexico + 52 1 (55) 5559 firstname.lastname@example.org
(C) 2015 iLS Clinical Research
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