About DAKA Consulting
DAKA Research Consulting was founded to help physicians confidently build and grow clinical research programs within their practices. With over 25 years of hands-on experience in clinical research operations and compliance, we provide practical, structured guidance from study startup through full regulatory support. Our goal is to make the research process clear, organized, and sustainable so physicians can focus on patient care while expanding their impact through research.
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Our Services
Clinical Trial Startup
We guide physicians through the complete process of launching a clinical research program, including feasibility assessment, site preparation, and operational planning.
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IRB & Regulatory Submissions
We prepare and manage Institutional Review Board (IRB) submissions, regulatory documentation, and compliance materials to ensure timely and accurate approvals.
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Compliance & Research Oversight
We provide ongoing regulatory compliance support, SOP development, and audit readiness to help practices maintain high research standards and operational integrity.
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SOP Development & Infrastructure Setup
We design structured workflows and standard operating procedures to build a sustainable research framework within your practice.
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Study Feasibility Assessments
We evaluate your practice’s readiness for clinical research and identify the right study opportunities aligned with your specialty.
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Research Program Consulting
Strategic consulting to help expand, improve, and optimize your existing clinical research operations.
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Have questions about launching or strengthening your clinical research program? Complete the form below and we will respond within one business day.
















