Services at CLINIC RESEARCH OF TAMPA BAY

1. Participant Recruitment and Screening

◦ Identifying eligible participants.

◦ Conducting thorough medical screenings.

2. Informed Consent Process

◦ Educating participants about the study.

◦ Ensuring ethical and legally valid consent.

3. Study Coordination and Management

◦ Scheduling participant visits and activities.

◦ Managing study timelines and adherence to protocols.

4. Data Collection and Documentation

◦ Recording accurate data for analysis.

◦ Ensuring high-quality, compliant data management.

5. Study Drug Administration and Monitoring

◦ Administering investigational products.

◦ Monitoring participant safety and treatment efficacy.

6. Lab Sample Collection and Processing

◦ Collecting and processing biological samples.

◦ Ensuring proper storage and regulatory compliance.

7. Regulatory Compliance and Reporting

◦ Adhering to Good Clinical Practice (GCP) guidelines.

◦ Submitting reports to sponsors, IRBs, and regulatory agencies.

8. Participant Care and Follow-Up

◦ Providing ongoing medical oversight.

◦ Conducting follow-up assessments and visits.

9. Quality Assurance and Monitoring

◦ Conducting internal audits and inspections.

◦ Collaborating with sponsors to maintain compliance.

Mission: To deliver state-of-the-art clinical trial services that drive medical advancements, improve lives, and shape a healthier future for our community and beyond.