Welcome to Cutting C Consulting LLC
Expert Consulting Services with Steven Curley, M.D., F.A.C.S.
Services Provided
Put Dr. Curley's 35 years of experience to work for you. He is available to meet with hospital, cancer program, surgical, clinical research, start up medical drug and device, and biomedical industry leaders and key stakeholders virtually or in person. He can assist in all phases of cancer or surgical program design, implementation, and optimization of services; assist with improving clinical trial programs; and provide guidance in critical planning in the process of testing and commercializing novel therapeutic and diagnostic approaches.
Select any of the four areas below to learn more.
Design, Expand and Improve
Cancer Programs
Services include:
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Evaluation of new or existing cancer center plans, layouts, or designs to optimize delivery of care, improve patient access and increase operational efficiency.
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Meet with administrative leaders, physicians, nursing staff and other key groups to plan new cancer centers and programs.
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Review and recommend changes to improve surgical, medical, pharmacy, and diagnostic services for inpatient and outpatient facilities.
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Develop competitive marketing strategies to increase patient referrals and improve community awareness of available services and providers.
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Expand and improve prevention, screening, and ancillary patient wellness programs across hospital systems.
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Advise on hospital and clinical staff well-being programs to improve recruitment and retention of a more satisfied and supported group of care providers and facility support staff.
Optimization of Surgical Services
Services include:
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Thoroughly assess surgical patient flow, operating room staffing and efficiency, and opportunities to improve outpatient and inpatient surgical and procedure based services.
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Optimize operating room staffing levels to improve pre-operative, intra-operative, and post-operative surgical patient care.
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Assist in prioritization of capital expenditures for rapidly evolving and new surgical equipment and products.
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Recommend programs to improve patient safety and reduce errors in the operating room environment.
Enhance Clinical Trial Programs
Services include:
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Demonstrate areas to improve and grow clinical research programs that are relevant for patients with malignant and non-malignant disease.
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Discuss cancer research database development and maintenance.
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Prioritize clinical trial offering based on regional cancer incidence and patient access.
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Connect hospital and cancer programs with pharmaceutical and medical device companies, clinical trial groups, and burgeoning diagnostic imaging, genetics, biomarker and multi-cancer early detection blood testing services to participate in cutting edge clinical trials.
Pre-Clinical
Research and Clinical Trial Design
Services include:
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Share 35 years of experience in developing and testing novel drugs, diagnostic modalities, and medical and surgical devices with established pharmaceutical and medial device companies, and academic researchers regarding bench, pre-clinical, and clinical testing, all based on GLP procedures.
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Advise on nanotechnology and nanomaterials used in cancer diagnostic and therapeutic applications.
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Review FDA submission requirements and assist with FDA and CMS approval processes for novel drugs and devices.
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Develop and draft research protocols, pre-clinical studies, and clinical trials for novel drugs and devices.