Integrating clinical research into established healthcare operations with training, transparent feasibility, regulatory guidance, and dedicated management support.
AMD Clinical Research partners with physicians, dentists, and specialty healthcare providers to incorporate clinical research into their existing practices. We support the research component—from evaluating opportunities and coordinating training to managing research workflows and providing ongoing operational guidance—while our partners continue delivering their established patient care services.
We identify and engage established physician-led practices, dental practices, and specialty healthcare providers interested in adding clinical research. We assess clinical expertise, existing patient populations, and operational needs, then work collaboratively to plan a research program that complements each practice’s current services.
We coordinate Good Clinical Practice (GCP) training and provide practical education on investigator responsibilities, protocol adherence, informed consent, source documentation, safety reporting, and day-to-day trial processes. Training and ongoing guidance are tailored to each practice’s research experience.
We use structured feasibility questionnaires and transparent assessments to evaluate patient populations, staffing, equipment, therapeutic expertise, and recruitment potential. Our goal is to communicate realistic capabilities to sponsors and CROs and help practices prepare for appropriate study opportunities.
We support essential-document organization, training records, delegation processes, and study-specific compliance workflows. We also educate site personnel on Institutional Review Board (IRB) oversight, centralized IRB processes, and inspection-readiness expectations, with an emphasis on continuous preparedness.
AMD supports research workflow development, staff coordination, documentation oversight, study tracking, sponsor/CRO communication, and operational problem-solving. We remain engaged during study conduct and can provide responsive, day-to-day support when needed.
We help connect qualified investigators and established practices with potential clinical trial opportunities, prioritizing transparent feasibility, appropriate study fit, research quality, and collaborative communication. Study selection and participation remain subject to sponsor/CRO review and approval.
Our model is designed to support an additional research function within an existing practice—not replace its clinical services. Investigators retain their clinical and regulatory responsibilities, while AMD provides dedicated research operations support.
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