BIMO PRO (The Quality Maven, LLC) was founded by Camille Brown, a former FDA Bioresearch Monitoring (BIMO) Investigator with more than 15 years of industry experience and almost 10 years of experience conducting FDA inspections. Since then, she has expertly strengthened this regulatory foundation with leveraged consulting opportunities across the U.S. and internationally.

Drawing on her deep global expertise in Good Clinical Practice (GCP), compliance strategy, and regulatory inspection readiness, Camille saw a need for smarter, more proactive quality solutions for pharmaceutical and medical device sponsors and their stakeholders in navigating today’s complex clinical trials landscape.

Cue BIMO PRO.

We deliver strategic quality consulting that blends technical rigor, operational efficiency, and a strong ethical foundation. We don’t just help you pass inspections—we help you build processes that scale and raise the standard for clinical excellence.

With a no-nonsense, analytical approach, BIMO PRO blends technical rigor with a strong ethical foundation. We take a pragmatic stance to help your organization raise quality standards and stay on top.

What We Do Best

• FDA BIMO Inspection Readiness & Remediation Strategy

• GCP audits: Investigator sites, CROs, Vendors, and Sponsor Mock FDA BIMO

• Strategy Development for Risk-based Quality Management (RBQM), Quality by Design (QbD) & CAPA Oversight

• SOP Development

• Training and Coaching for Cross-functional Teams

Our Foundation

From A to Z, every engagement is grounded in our core values:

• Integrity in every recommendation

• Precision in every audit

• Partnership with every client

Certifications & Expertise

• 10 years as an FDA BIMO Investigator

• 15+ years of clinical research and quality assurance experience

• Deep expertise in GCP, inspection readiness, and regulatory strategy

• Global experience auditing clinical investigator sites, CROs, vendors, and sponsors