Yes, and keeping the two properly separated is a core part of what we do. Many memory clinics participate in Alzheimer’s and dementia research, and trial data must stay segregated from the clinical EHR to meet sponsor, IRB, and regulatory requirements. We design network segmentation, access controls, and secure storage so research systems do not mix with protected clinical records, while both remain backed up and recoverable. We also support secure data transfer to sponsors and coordinating centers. This lets your clinic run trials confidently without putting patient care data or HIPAA compliance at risk.