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Pharma R&D and Real World Evidence Studies
Medical Writting
Clinical Monitoring and Project Management: Comprehensive Oversight
Country and Site Feasibility: Optimizing Trial Locations
Regulatory and Ethics Approvals
Biostatistics and Data Management
Quality Assurance: Inspection-Ready Trials
Study&Site Start-up: Ensuring a Seamless Launch
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Medical Device Studies
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Application for Conformity Assessment
PMS and PMCF activities
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