MedApex Research can assist your company with clinical trial planning and design in many areas prior to executing the clinical trial itself, such as:
● Clinical trial protocol design and development - to ensure alignment with FDA requirements and industry standards
● Pre-clinical trial strategy and tactic development (for Pharmaceutical and Medical Devices)
● Clinical trial strategy and timelines development (for Pharmaceutical and Medical Devices)
● Clinical trial feasibility and costs planning
● Patient recruitment and site selection through our extensive network of hospitals, clinics, and research institutions
● Comprehensive regulatory submissions, including Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications