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.
Study Start up and Regulatory Services.
SAP (Statical Analysis plan)
Monitoring - Phase 1 to Phase 4 studies.
Import and export services.
Outsourcing of specialized staff.
Data Management and Central Laboratories.
Consultancy on LA Clinical Research Processes.
Staff training .
Matías Romero 102, Int. 205
Del Valle, Ciudad de México, 03100México
(C) 2015 iLS Clinical Research
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