Ag Biotech and Gene Editing innovations face complex, multi-jurisdictional regulatory pathways—from trait discovery to global approvals. We help developers navigate each step with precision, integrating science, policy, and commercial strategy to minimize risk and accelerate success.
Navigating regulatory requirements for chemical inputs demands precise data and strong justification. From exposure modeling to dossier Q&A, we guide clients through study design, risk assessment, and global registration strategies.
From fermentation-derived proteins to novel enzymes, we guide feed innovations through global safety reviews and regulatory approvals, streamlining submissions and securing confidence with both regulators and investors.
Biological products face unique challenges in regulatory classification and safety justification. We help developers frame biologicals, microbial consortia, and soil inputs with rigorous science tailored to emerging global standards.
We support innovators working with gene-edited, microbial, and GMO-derived food ingredients—crafting defensible safety assessments and regulatory strategies to enable market access and commercial success.