Services

 

We share our expertise with teams who would like additional support in research and development, scientific communications, funding proposals, and project management efforts.

 

 

 

 

 

~ Data Interpretation and Scientific Communication ~

Translate scientific data into audience-specific materials to support understanding, decision-making, and engagement

 

Examples

Project summaries for commercial teams

 

Content for regulatory submissions to the FDA

 

Portfolio presentations to cross-functional teams and executives

 

Funding proposals to government agencies (e.g., DoD, BARDA, NIH)

 

Review articles for animal welfare organization members

 

SOPs for manufacturing and quality teams

 

Peer-reviewed manuscripts for public

 

 

 

 

 

~ Program Support and Strategy Planning ~

Provide structure, planning, and strategic direction to advance science-based programs

 

Examples

Create regulatory strategies to transition projects through development

 

Manage multiple technical projects across external stakeholders and partners 

 

Create standardized data collection tools to support program evaluation and improvement

 

Provide data-driven recommendations to strengthen canine enrichment initiatives

 

Prioritize R&D projects based on scientific data analysis and literature reviews

 

Implement risk mitigations during product development

 

 

 

 

 

 

Some of Our Ripplets

Examples of our work and their impact

 

Positioning Therapeutic Innovation for External Funding

Breanne collaborated with cross-functional teams to develop several funding proposals supporting medical countermeasure initiatives.  She designed content that connected unmet medical needs with project objectives, development plans, technical feasibility, and anticipated outcomes.  By aligning complex scientific and regulatory information with the priorities of government and public-sector organizations, she helped communicate the value and readiness of the science and teams, resulting in external funding for 3 programs.

 

Translating Research into Therapeutic Projects

Breanne advanced the scientific understanding of immune pathways by designing, conducting, and analyzing experiments across immunology and related fields. She interpreted complex data into clear communications for academic and cross-institutional teams, resulting in peer-reviewed publications, conference presentations, and funded grant proposals. 

 

Applying Scientific Insight to Regulatory Success

At a pharmaceutical leader of auto-injectors, Breanne helped expand development pipelines and commercial product lines by conducting thorough literature searches and evaluating scientific evidence to guide regulatory strategies. She applied rigorous due diligence to assess technical feasibility, regulatory viability, and compliance.  This evidence-driven approach enabled clear decision making, strengthened portfolio development, and supported publication readiness while maintaining alignment with U.S. regulatory standards.  

 

Expanding Regenerative Medicine Allograft Portfolio

While leading R&D efforts at a global nonprofit organization, Breanne collaborated with cross-functional teams to launch 2 osteobiologic allografts and simultaneously directed 5 concurrent projects, transferred production processes, and built lifecycle strategies to meet unmet clinical needs. By integrating scientific analysis with clear documentation, she advanced innovation while ensuring compliance, scientific integrity, and cross-functional alignment, resulting in an expanded commercial portfolio and stronger research pipeline.

 

Educating Animal Behavior Consultants

Breanne elevated the standards of animal behavior consulting by making science more accessible and actionable for professionals.  She translated research into clear content that bridged academic findings and practical application to support better understanding, collaboration, and decision-making for animal behavior programs.

 

Aligning Stakeholders and Regulatory Processes

Before creating BioRipplet Endeavors LLC, Breanne managed 15+ regulatory and nonclinical workstreams across 4 drug-device combination product programs, aligning stakeholders and the FDA to create clear decision pathways, and accelerate submission readiness. At the same time, she sustained compliance for 2 FDA-approved products by managing 8 post-marketing requirements and coaching colleagues for consistent delivery. This resulted in on-time execution, reduced rework, and strengthened scientific credibility.