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Clinical Research

KenKor 360's customized regulatory support services for clinical research compliance help ensure adherence to Good Clinical Practice (GCP), regulations, guidelines, and specifications relevant to business processes. We are experienced in all phases of development and are committed to ethical conduct that yield high quality assurance standards in clinical research management.

We Start With an Assessment

Risk assessment is an essential piece of clinical trial management. Identifying and evaluating events that could impact the achievement, timeline, and study objectives is a continuous and systemic process. Our risk management assessment includes a personalized consultation with a KenKor 360 advisor who will interview your team to understand your organizational and program goals, current processes in place, and ensure best practices are being followed. Our team will partner with your organization to provide advisory and tailored support in areas such as:

-Regulatory documentation

-Submission process, planning, and development

-SOP design, administration, and compliance

-Trial Master File (TMF) management

-Clinical quality plans

-Clinical vendor oversight

-Risk assessment process


-Inspection readiness plans