Supplements Clinical Services
IRSI is a full service clinical research site. Services can be added or removed to a clinical study as needed to fit our Sponsor’s needs.
- Claims review
- Protocol development
- Clinical study document development (Protocols, Case Report Forms, Diaries, Questionnaires, Instructions)
- Study conduct
- Expert assessments, instrumentation, phlebotomy, routine and unique laboratories, photography and image analysis
- Statistical Analysis (plan and conduct of analyses)
- Quality Control / Quality Assurance (off site QA team reviews documents as well as data)
- Coordination with Medical Investigators (Primary Care, OB/GYN, Endocrinologists, GI, GU, Dermatologist, Ophthalmologist)
- Coordination of IRB review and approvals
- Final Report Writing
- Presentations of study results
