Patient Recruitment

Patient recruitment is a critical aspect of clinical trial success, yet it can be one of the most challenging and time-consuming tasks.

The investigator identifies potential participants who meet the eligibility criteria outlined in the study protocol. This may involve reviewing medical records, electronic health records (EHRs), patient databases, or collaborating with other healthcare providers to identify eligible candidates.

Once informed consent is obtained, eligible participants are enrolled in the study and scheduled for study visits according to the protocol. The investigator ensures that participants receive appropriate instructions and guidance regarding study procedures, medication administration (if applicable), and follow-up appointments.

Our quality department audits the recruitment process to ensure the recruitment process complies with GCP, ethics committee, and local authority guidelines.