RGM brings the perspective of someone who has built and led the work — not just advised on it.
What We Do
RGM brings senior operating judgment to moments where the path is complex, the risk is unclear, or the organization needs to move faster. We help companies translate scientific and regulatory complexity into actionable product, claims, evidence, launch, portfolio, and transformation decisions — so teams can align, act, and move forward with confidence. Built from experience leading the work — not just advising on it.
Our Promise
For decision-makers: we translate complex regulatory and scientific requirements into clear, actionable guidance that can be used inside a real organization — to make decisions, align stakeholders, and move forward with confidence.
For regulatory & scientific teams: RGM helps teams strengthen their role as strategic partners to the business — improving how decisions are framed, how risks are communicated, how priorities are set, and how regulatory work is connected to business outcomes.
The Founder
Founder & Principal
RGM is led by Raquel Mura, a global regulatory, scientific, and transformation executive with decades of leadership experience inside major life sciences and consumer healthcare organizations — including Sanofi Consumer Healthcare, Sanofi R&D North America, Reckitt, and Pfizer Nutrition.
Over her career she has built and led a global regulatory organization of approximately 170 colleagues, directed R&D operations representing more than 2,000 scientists, led regulatory due diligence and integration across major consumer health transactions, and delivered a first-in-class Rx-to-OTC switch. Her work spans regulatory affairs, R&D operations, innovation and new product development, claims and evidence strategy, and digital and AI transformation.
That breadth — regulatory, scientific, commercial, and organizational — is unusual in a single advisor, and it shapes how RGM approaches every client question: not as an isolated regulatory issue, but as a business decision with product, evidence, launch, and organizational implications.
She is also a member of the faculty at Rutgers University, teaching Fundamentals of Regulatory Affairs in the Master of Science and Master of Business and Science programs, and advising graduate students preparing for careers in regulatory and life sciences.
Academic
Faculty Member — Master of Science and Master of Business and Science programs at Rutgers University →
Leadership Experience
Led global regulatory strategy for 20+ brands across OTC drugs, Rx-to-OTC switch, food supplements, medical devices, and cosmetics. Designed a new operating model and governance framework for a team of approximately 170 colleagues.
Represented more than 2,000 scientists. Led major R&D operations, site strategy, and governance for transversal digital and AI initiatives. Co-led companywide change management blueprint and best-practice development for R&D M&A integration.
Led regulatory due diligence for major consumer healthcare acquisition activity and a first-in-class Rx-to-OTC switch partnership. Designed and implemented a new regulatory operating model.
Led global cross-functional innovation work, delivered new product concepts, and contributed to maternal health launches. Direct commercial and innovation strategy experience inside a global consumer health organization.
Teaches Fundamentals of Regulatory Affairs and advises graduate students. Brings current industry practice, FDA precedent, and innovation perspective into the classroom.
Built experience across dietary supplements, nutritionals, medical foods, infant formula, consumer healthcare, and multiple geographies, including Latin America, Europe, and the U.S.
What this means for clients
Raquel has built the organizations, led the teams, managed the cross-functional decisions, supported the transactions, navigated the regulatory and innovation questions, and now teaches the next generation of professionals on the same topics RGM helps clients address. The advice is informed by execution, not abstraction.
By the Numbers
~170
Colleagues in a global regulatory organization built and led by the founder
2,000+
Scientists represented in R&D organizations led globally
3,000+
Marketing authorizations managed in transaction diligence and integration
Categories We Work Across
Consumer healthcare, biopharma, dietary supplements, medical devices, women's health, OTC and non-prescription products, and adjacent categories — including products that do not fit neatly into one box.
