Advancing Research. Bridging Expertise. Championing Progress.
At Third Coast Regulatory Solutions, we help academic researchers, organizations, and life sciences innovators navigate the complexities of medical product research and development—efficiently, strategically, and with confidence.
Accelerating the journey from Academic Discovery to Real-World Impact
With deep roots in the Texas Medical Center—the world’s largest medical complex and most efficient life sciences ecosystem—and strong ties to top-tier academic research institutions and stakeholders nationwide, we bring unmatched insight and connectivity to your team.
We work alongside you, fostering impactful collaborations to bridge the gaps within your organization, simplifying compliance and generating momentum across your research and development efforts.
In a landscape defined by shifting priorities, resource constraints, and evolving needs, we provide flexible, high-level expertise that helps you adapt, stay aligned, and continue advancing toward your goals.
Translating innovative research into clinical applications and market-ready products requires more than great science— it demands a steady anchor and strategic driver to propel projects forward in an ever-evolving environment.
From early discovery through commercialization, we help research teams navigate the complexities of product development and regulatory strategy with clarity and confidence.
Whether you're advancing a novel therapy, medical device, digital health tool, or institutional initiative, our support is tailored to meet your emergent needs—empowering you to move efficiently from concept to impact.
Strategic Support for Translational Research and Product Development
Our Areas of Expertise
Fractional Regulatory Affairs Support
Access the senior-level regulatory leadership you need, when you need it—without the burden of sourcing, onboarding, and maintaining a full-time position.
We provide hands-on leadership and support for engagements with regulatory bodies to keep your projects on track and aligned.
Clinical Translation Management
From preclinical proof-of-concept to early-phase trials, we help bridge the gap from bench to bedside.
We guide you through the clinical translation process with regulatory precision and operational insight, minimizing the potential for costly delays and optimizing your path to impact.
Research Operations & Administration
Inefficiencies in research operations and research administration slow progress.
We strengthen your internal infrastructure—optimizing workflows, minimizing bottlenecks, aligning teams, and streamlining study startup—so your research can move forward efficiently and effectively.
Compliance & Inspection Readiness
Stay inspection-ready and aligned with local, federal, and international regulatory requirements and standards.
Our proactive compliance support reduces regulatory risk, promotes reliable, audit-ready documentation, and positions your programs for long-term success.
A Message from Our Founder & Principal
"Regulatory, administrative, and operational barriers shouldn’t stand in the way of groundbreaking research and innovation—but too often, they do.
I founded Third Coast because I’ve seen firsthand how the right strategic guidance and hands-on support can mean all the difference between stalled progress and tangible, real-world impact.
I’ve dedicated my career to working alongside leading research institutions, healthcare systems, and life sciences innovators to transform research and product development hurdles into milestones for success. I know the challenges you face—because I’ve been in the trenches solving them.
At Third Coast, we don't just consult. We become part of your team— bringing deep experience, operational leadership, and tailored solutions to the table. Whether you're advancing drugs, devices, biologics, or other emerging medical products, tools, and technologies, we help you move forward with clarity, compliance, and efficiency.
Because when research moves forward, so does patient care, innovation, and the future of healthcare."
– Eva Zimmerman, MCTM, CCRP, CPGP, RAC-US
Expertise Built within the Nation's Top Research Institutions
The insight behind every Third Coast engagement stems from over a decade of direct experience inside some of the nation’s most respected academic, clinical, and research organizations—where we gained a deep understanding of what it truly takes to advance innovation and move research forward.
What Our PARTNERs Say
“Extraordinarily helpful and efficient.”
Dr. Emily Carter
“Made everything as easy as possible.”
Mark Thompson
“Ridiculously good at project management.”
Sarah Johnson
“Support from people like Eva makes a huge difference for our odds of success.”
David Lee
How We Work Together
1. Connect with Us
Schedule a no-cost discovery call to discuss your goals and how we can help.
2. Tailored Engagement
We’ll define a customized Scope of Work and provide a Master Services Agreement to formalize our partnership.
3. Kickoff & Ongoing Support
Once onboarded, we’ll host a kickoff meeting, establish regular check-ins, and provide consistent progress updates.
4. Final Deliverables & Review
Every engagement concludes with a complimentary post-project review to gather feedback and identify future opportunities. Our goal is to foster long-term collaboration and provide ongoing support to help your research thrive.
Let's talk!
Business Hours
- Mon - Fri
- -
- Sat - Sun
- Closed
📍 Based in Texas, Serving Clients Worldwide
Contact Us
Thank you for reaching out to Third Coast Regulatory Solutions! We're excited to learn more about your goals and how we can support your research and development efforts.
You’ll hear from us shortly—usually within one business day. In the meantime, feel free to explore our capabilities or connect with us directly by sending an email to Eva@ThirdCoastRegulatorySolutions.com.
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