Site and Patient Access
Open the Door to Efficient Enrollment

Site Access
Choosing the right sites for a clinical study can determine your success. At Kernel, we prioritize robust site evaluation. By leveraging performance metrics and real-time data, we ensure that every clinical study is matched with the most suitable investigator sites at every stage. This data-driven approach boosts productivity, efficiency, and overall quality.

Our Subject Recruitment Services
Targeted Recruitment Planning
Defining study-specific eligibility criteria and outlining effective strategies for diverse populations
Enrollment & Screening Management
Assigning unique subject IDs, maintaining screening logs, and integrating demographic data into an Electronic Data Capture (EDC) system.
Informed Consent Process
Providing IRB-approved forms in accessible language, ensuring voluntary participation and compliance with Kernel Center SOPs.
Participant Follow-Up & Retention
Proactively tracking participant engagement, study integrity, and safety adherence.
Regulatory & Ethical Compliance
Ensuring all recruitment materials receive IRB approval before implementation.
Multi-Channel Recruitment
Leveraging electronic health records (EHRs), referrals, advertisements, and patient support groups to maximize outreach.
Patient Enrollment
Efficient and ethical subject recruitment is critical to the success of any clinical trial. Kernel CRO implements an IRB-approved, participant-focused recruitment process that ensures timely and effective enrollment while maintaining compliance with ICH-GCP and ethical guidelines. Our medical teams ensure efficient monitoring of any side effects while protecting patient confidentiality and privacy under HIPAA standards.

At Kernel, we’re building a future where innovation and excellence go hand in hand.
Interested in partnering with us as a site?
Contact us or visit our site-registration portal to learn more about eligibility and collaboration opportunities.