Consults in Policy and Medical Devices

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About us

Trusted Leadership

Dr. Peter D. Rumm provides consulting services to policy makers and medical device companies. With decades of leadership in the FDA, military health, and public health policy, He offers unique expertise to help clients with complex policy or regulatory issues or to help guide device manufacturers through the process to get a device on the market.    His expertise includes clinical trial evaluation and advice.

Strong Integrity

We uphold transparency, honesty, and ethical practices in every consultation, ensuring trusted and compliant guidance for your success.

Genuine Care

We prioritize your goals with sincere dedication, offering personalized support and solutions that truly reflect your needs.

Experience that Sets Him Apart

With decades of leadership in health policy, military medicine, and medical device regulation, Dr. Rumm brings unmatched insight and trusted expertise to every consultation.
Military commander and senior epidemiologist, state chief medical officer, academic center director, FDA deputy director of divisions, duties at the US Surgeon General Office and recently retired as a national policy director at the VA.
Has commanded or led military facilities, and worked in over a dozen countries. Led a14 country course on preparedness in Macedonia.
Over a hundred local to international level lectures, holds two faculty positions as an adjunct associate professor.
Many military awards, distinguished service award at VA, Columbus State University Distinguished Alumni Award, and the Order of Malta from the Military Service of Italy.

Our Mission

Our mission is to bridge the critical gap between science, policy, and innovation by providing expert guidance to medical device companies, public health institutions, and policy makers. In an ever-evolving regulatory landscape, we help organizations navigate complex healthcare regulations, approval processes, and ethical frameworks with clarity and confidence. Through evidence-based insights and strategic support, we promote public health solutions that are not only effective and safe but also aligned with the highest ethical and scientific standards. We are committed to advancing health equity, regulatory transparency, and innovation in service of better outcomes for patients and communities.

Our Vision

We envision a healthcare and regulatory ecosystem where sound policy, scientific rigor, and practical innovation work together to improve the lives of people everywhere. Our vision is to be the leading consulting resource for stakeholders seeking trusted, experienced, and mission-driven guidance in the fields of public health policy and medical technology. We aim to influence meaningful change by supporting decisions that are rooted in truth, guided by experience, and centered on the wellbeing of all. By aligning the goals of industry and government, we seek to build systems that are forward-thinking, resilient, and responsive to emerging public health needs.

What We Do

We provide expert consulting in medical policy, regulatory pathways, and device approval processes. Led by Dr. Peter D. Rumm, our services include:
  • Strategic advice for navigating FDA requirements
  • Clinical trial evaluation and readiness
  • Public health policy development
  • Support for government, academic, and private sector initiatives
  • Crisis and emergency policy guidance

Our Goal

Our goal is to empower healthcare organizations, medical device innovators, and policy makers with the tools, knowledge, and strategic direction needed to bring life-saving technologies to market while upholding the highest standards of public health policy. We seek to make the regulatory journey less daunting and more productive—ensuring that each step, from concept to compliance, is met with expert insight and support. Ultimately, we aim to drive sustainable progress in global health by fostering collaboration, improving access to regulatory expertise, and contributing to smarter, safer healthcare systems for future generations.
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