Your Vision, Our Mission

**Coming soon** A technical skills training and certification program that upskills students, early-career professionals, and transitioning workers. Skills Trained: • Current Good Manufacturing Practice (GMP) & Quality Systems • Process Validation, Risk Management, and Data Integrity • Biomanufacturing Operations & Regulatory Compliance • Leadership, Project Management, and Technical Sales • Vendor Oversight & Digital Quality Documentation

Comprehensive engagement for early founders or small businesses covering discovery/solution assessment, regulatory roadmap, translational business strategy, supply chain planning, and investor/funder readiness package.

A one-time evaluation of a researcher’s candidate molecule or technology. Includes regulatory fit analysis, early feasibility, and a roadmap of next steps.

University career counseling centers, tech transfer offices or startup accelerators purchase a block of readiness assessments and advisory hours for their students, or cohorts of researchers/founders.

At F2i Partners, we believe knowledge is the first step in bridging the gap from ivory to industry. Our training and workshops are designed to equip early career professionals, academic researchers, startups, and universities with the tools and insights needed to upskill, navigate regulatory strategy, and the biotech industry. Each program is practical, accessible, and tailored to help turn early potential into real world success.

F2i Partners provides strategic consulting to help innovators move beyond the lab and into real-world application. We advise on regulatory readiness, quality by design, validation frameworks, supply chain strategy, and commercialization pathways. Our role is to simplify complex requirements, de-risk early biotech ventures, and give researchers and startups a clear, actionable roadmap.

Engineers provide guidance across the full validation lifecycle, helping ensure suppliers, manufacturers, processes, systems, and facilities meet production capability and regulatory expectations. Our services include Validation Master Planning, IQOQPQ protocols, and process validation utilizing Quality by Design (QbD) approaches.

We aim to provide strategic and operational support to transform valuable ideas into viable ventures. Our business support services include startup formation guidance, business plan development, and go-to-market strategy tailored to biotech and life sciences. We help teams navigate intellectual property considerations, align with funding opportunities such as SBIR/STTR grants, and build investor-ready pitch materials. We act as a partner at the intersection of science and business.

Qualification of vendors and suppliers for raw materials, consumables, and critical equipment. Risk-based assessments to ensure quality, reliability, and regulatory compliance. Ongoing monitoring of supplier performance, corrective action tracking, and documentation review.

Support in selecting contract partners for research, clinical, and manufacturing activities. Gap assessments of partner facilities, processes, and quality systems. Review of validation and GMP documentation to ensure alignment with sponsor expectations. Ongoing oversight during project execution to reduce risk of delays, compliance issues, or FDA findings