Real-World Evidence (RWE) Research
Teamit has extensive experience supporting multi-country RWE studies in collaboration with pharmaceutical companies, academia, healthcare professionals, policymakers and regulatory agencies. Our scientific expertise in RWE and strong project management skills ensure successful study planning, implementation, and delivery.
Study design and fit for purpose
Collaborate on protocol development, feasibility studies, and data partner selection.
Study implementation and regulatory compliance
Plan, implement, and close-out studies; ensure regulatory compliance, obtaining necessary approvals.
Reporting and data management
Ensure timely data collection and efficient data management, reporting, and presentation of results to studies’ sponsors.
Risk management and quality assurance
Identify and manage risks, implement mitigation strategies, and ensure quality assurance.
Contracting and financial management
Manage study budgets, negotiate contracts, and handle financial aspects.
Hands-on Experience
We are currently participating in over 10 studies sponsored by EMA or pharmaceutical companies and have contributed to other four which are now closed. Ultimately, all these studies aid in decision-making regarding treatment strategies, patient care, as well as the benefit/risk monitoring of marketed medicinal products.
