Bravado Pharmaceuticals

Bravado Pharmaceuticals Bravado Pharmaceuticals is a full service contract research organization.

The company has capability to develop virtually any type Pharmaceutical dosage form on a contract basis.

02/06/2026

Please welcome Dr. Kelsey McMillan to Bravado Pharmaceuticals as a consultant!🎉

Dr. Kelsey McMillan has joined the Bravado Pharmaceuticals Team as a consultant. Kelsey has previously worked as a Clinical Research Assistant at the Ohio State University in the Comprehensive Cancer Center. As one of only 49 designated comprehensive centers in the Nation – Arthur G. James Cancer Center and Richard J. Solove Research Institute is “dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. Applied discoveries are used to develop more effective approaches to cancer prevention, diagnosis and therapies – providing tomorrows standard of care today”. The statement in her employment letter years ago says, “A Cancer-Free World Begins Here, Welcome to the OSU CCC!”. Kelsey is currently a first-year resident at Duke Medical Center, Raleigh, NC with goals to complete her residency in Oncology over the next two years.

Kelsey’s Academic Background:
• Freedom HS, Tampa Palms, FL
• BS in Biochemistry, The Ohio State University (Minor in Pharmaceutical Studies)
• MS in Pharmacology, The Ohio State University
• PharmD, The Ohio State University

02/05/2026

We’re excited to welcome Luis Adorno to the Bravado Pharmaceutical team! 🎉

Luis G. Adorno is a pharmaceutical operations and quality leader with more than 24 years of progressive experience across global manufacturers, CDMOs, and FDA-regulated commercial pharmaceutical environments. Now serving as Director of Manufacturing & Quality at Bravado Pharmaceutical, he brings a proven record of building compliant, high-performing operations that consistently deliver product quality, inspection readiness, and scalable manufacturing ex*****on.

Luis’s career has been defined by leading at the intersection of ex*****on and governance—where manufacturing performance must align with rigorous quality systems. He has directed cGMP manufacturing and packaging operations supporting both clinical and commercial products, with hands-on command of solid and liquid dosage forms, blistering, bottle lines, serialization, and complex equipment platforms. His technical depth includes equipment qualification (IQ/OQ/PQ), cleaning validation, environmental monitoring, batch record governance, and contamination-control fundamentals—enabling him to translate regulatory expectations into practical, sustainable controls on the floor.

A recognized authority in pharmaceutical quality systems, Luis leads investigations and remediation with discipline and clarity. He drives structured root-cause problem solving, ensuring CAPAs are measurable, risk-based, and built to prevent recurrence—not simply close events. His leadership reinforces ALCOA+ data integrity as a daily standard, strengthening the reliability of batch documentation, laboratory records, and operational decision-making. Across multiple organizations, he has helped establish inspection-ready cultures through clear ownership, high training standards, and effective management of change.

As a people leader, Luis has directed teams of up to 35 across Manufacturing, Quality, Engineering, and EHS, developing operators and supervisors into confident, compliant performers. He is known for creating accountability without sacrificing engagement—building teams that execute with discipline, think critically, and respond effectively under audit and production pressure.

Welcome to the team, Luis—we’re glad to have you! 💙💊

February is American Heart Month. We’re proud to support the science behind safe, effective therapies that help improve ...
02/04/2026

February is American Heart Month. We’re proud to support the science behind safe, effective therapies that help improve and protect heart health. Every test, every method, every result matters.

January set the tone — focused, compliant, and driven by excellence.We’re ready for what’s next.
01/30/2026

January set the tone — focused, compliant, and driven by excellence.

We’re ready for what’s next.

Documentation isn’t just paperwork — it’s proof of quality, traceability, and accountability.
01/28/2026

Documentation isn’t just paperwork — it’s proof of quality, traceability, and accountability.

As January comes to a close, we remain focused on advancing quality, efficiency, and innovation throughout 2026.
01/26/2026

As January comes to a close, we remain focused on advancing quality, efficiency, and innovation throughout 2026.

Big progress happening behind the scenes!Our President and CEO, Brian McMillian, has been on the move—most recently trav...
01/22/2026

Big progress happening behind the scenes!

Our President and CEO, Brian McMillian, has been on the move—most recently traveling to Louisville, Kentucky to meet with the Kentucky Board of Pharmacy as part of our multi-state licensing efforts.

Our goal is ambitious: licensure in all 50 states to distribute product nationwide. In just a couple of months, we’ve already achieved licensure in nearly 20 states—an incredible milestone and a testament to our team’s momentum. 🚀

More to come as we continue expanding our reach.


Today we honor Dr. Martin Luther King Jr. and his legacy of integrity, service, and purpose — values that guide our work...
01/19/2026

Today we honor Dr. Martin Luther King Jr. and his legacy of integrity, service, and purpose — values that guide our work every day.


Innovation in pharma isn’t defined by novelty alone—it’s measured by trust. True advancement comes from solutions that p...
01/16/2026

Innovation in pharma isn’t defined by novelty alone—it’s measured by trust. True advancement comes from solutions that perform consistently, deliver reproducible results, and stand up to regulatory scrutiny every time. At its core, meaningful innovation bridges scientific progress with validated processes, strong data integrity, and compliance by design—so new ideas don’t just move fast, they move forward with confidence and reliability.


📈Training & GrowthContinuous training is how we protect quality, strengthen compliance, and stay ahead of what’s next. A...
01/16/2026

📈Training & Growth

Continuous training is how we protect quality, strengthen compliance, and stay ahead of what’s next. At Bravado Pharmaceuticals, learning is built into our culture—so our teams remain knowledgeable, audit-ready, and equipped with the latest scientific and regulatory best practices. Because in a field that never stands still, neither do we.


Strong processes don’t happen by chance.At Bravado Pharmaceuticals, process excellence is intentionally designed—rooted ...
01/15/2026

Strong processes don’t happen by chance.

At Bravado Pharmaceuticals, process excellence is intentionally designed—rooted in thoughtful planning, rigorous validation, and clear accountability at every stage. From concept to ex*****on and continuous review, each step is aligned to uphold GMP compliance, data integrity, and patient safety.

Our approach in action:
📋Plan – Define clear objectives, risks, and controls before work begins
🛡️Validate – Confirm systems and methods perform as intended, every time
⚙️Execute – Operate with precision, consistency, and documentation
🔍Review – Analyze outcomes, drive improvements, and reinforce quality

Quality isn’t a checkpoint—it’s a lifecycle. And it’s how we deliver confidence in every result.

QA vs QCAt Bravado Pharmaceuticals, Quality Assurance (QA) ensures the systems behind our operations are designed, docum...
01/09/2026

QA vs QC

At Bravado Pharmaceuticals, Quality Assurance (QA) ensures the systems behind our operations are designed, documented, and executed correctly. Through robust procedures, training, and oversight, QA helps prevent issues before they arise and maintains compliance at every stage.

Quality Control (QC) ensures results meet established specifications through precise testing, monitoring, and analysis. QC provides the data-driven confirmation that our standards are consistently met.

Together, QA and QC form a unified quality framework that safeguards data integrity, supports regulatory compliance, and protects patient safety. This is what we do at Bravado Pharmaceuticals—delivering pharmaceutical excellence you can trust, every step of the way.

Address

4212 Cypress Gulch Drive
Lutz, FL
33559

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+18139914100

Website

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