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Bench to Bottle™ is our partnership model for supporting the full veterinary vaccine lifecycle. By aligning research, development, manufacturing, and regulatory perspectives from the start, it helps reduce handoffs, improve decision-making, and address downstream requirements earlier in development
In practice, partners can engage HRA for a specific stage of development or for end-to-end support. Throughout the program, teams keep manufacturing feasibility and regulatory expectations in view to support smoother execution..
HRA partners with organizations at various stages, from early-stage concepts to late-stage optimization, providing applied scientific support to generate meaningful, decision-ready data. Key collaboration areas include:
As programs progress, HRA supports robust, scalable, and transferable process design and optimization, including technology transfer planning and scale-up readiness for licensed products. This can be especially valuable for teams preparing for U.S. licensure or transferring products developed outside the United States.
HRA provides flexible manufacturing support that can be completed at HRA facilities or transitioned to a partner site following process development, helping maintain continuity between development and production.
Regulatory considerations are integrated throughout HRA’s approach, supported by scientific experience working with the USDA, helping teams align development strategies with U.S. regulatory expectations and reduce regulatory risk and uncertainty.
HRA was established in 2001 by Kristina J. Hennessy, DVM, PhD, Diplomate ACVM (Immunology), and is founded on principles of scientific rigor and regulatory integrity.
As part of Kemin, a family-owned company founded in Iowa in 1961, HRA benefits from long-term investment, global infrastructure, and established quality systems, supporting continuity as programs grow and scale.
Share your program stage and what you need next. We will connect you with the right HRA specialists.
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