Our regional support for you
knoell has local teams in the US and consulting partners in Canada to support local and global regulatory consulting and contract research organization (CRO) projects. knoell serves the regulatory and scientific needs of companies that range from multi-national Fortune 500 companies to start-ups. knoell USA-based affiliates access the full breadth of knoell experts globally to act as a full-service provider, by assembling a team to serve clients in crop protection and nutrition, biocides and antimicrobials, food and food contact materials, chemicals, and animal health.
Crop Protection and Nutrition
knoell USA supports registration and compliance consulting for a wide range of agricultural products, including biopesticides, conventional pesticides, fertilizers, biostimulants, soil amendments, adjuvants, and inert ingredients. knoell works with various regulatory agencies in North America to achieve desired outcomes for clients, including the US Environmental Protection Agency (EPA) under Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and Toxic Substances Control Act (TSCA), as well as Health-Canada’s Pest Management Regulatory Agency (PMRA) and the Canadian Environmental Protection Act (CEPA). knoell scientists and experienced regulatory professionals offer expertise in regulatory affairs, federal and state registration, dossier services, technical writing, quality assurance, and product stewardship. In addition to regulatory strategy, regulatory staff augmentation, and end-to-end registration services, knoell offers support with any step along the way, including study direction and monitoring as well as exposure modeling and risk assessment.
Biocides / Antimicrobials
In the US and Canada, biocides, antimicrobials, and preservatives are strictly regulated by US EPA under FIFRA and Health-Canada’s PMRA under CEPA. knoell offers a US-based team of experts to support your business through your products' life-cycle, ensuring FIFRA and PMRA observance, and supporting your company’s regulatory compliance. knoell has the experience to guide manufacturers, distributors, repackagers, and blenders at every stage of the biocides’ regulatory compliance process. knoell can help achieve the specific regulatory requirements of distribution, packaging, labeling, and relabeling of antimicrobials.
- Complete knoell service portfolio on Biocides/Antimicrobials!
Food and Food Contact Materials
knoell regulatory experts provide comprehensive solutions in the interpretation of global food contact regulations, implementation of required regulatory reviews and notifications, analytical testing, and toxicology assessments to ensure compliance and safe use of food contact materials.
- Complete knoell service portfolio on Food and Food Contact Materials!
knoell has a North America team of technical experts available to help businesses in the US and Canada navigate the heavily regulated field of chemical production, import, and use. knoell supports clients in complying with regulations on consumer and industrial products like chemical substances and mixtures, polymers, electric and electronic equipment, and home and personal care products.
knoell Animal Health provides regulatory and clinical trials expertise as well as services to support companies developing biologics and pharmaceuticals for veterinary use in the US. The 2020 acquisition of Triveritas, a globally recognized animal health contract research organization (CRO), established knoell’s footprint in the US. With staff working from within the Kansas City animal health corridor, knoell Animal Health is located in the same area as many of its clients.
Building on the strengths of fellow animal health members of the knoell family of companies, knoell Animal Health offers a full portfolio of services, including start-to-finish product development and ad hoc services. With established clinical teams in the US and Europe and over 750 years of animal health experience, knoell Animal Health can seamlessly coordinate projects in multiple geographies, from proof of concept to registration and beyond; balancing the three vital pillars of quality, time, and budget.
- Complete knoell service portfolio on Animal Heatlh
Our TSCA Support For You
- Strategic advice on test rules (TSCA Section 4)
- Development of PMNs (TSCA Section 5)
- Reporting for the CDR (TSCA Section 8(a))
- Development of TSCA 8 (c) Compliance Program
- Reporting of Substantial Risks (TSCA Section 8(e))
knoell main offices in the USA
knoell USA, LLC
2 Christy Drive I Suite 102
Chadds Ford, PA 19317
"knoell USA has supported me with complex submission documents, such as OECD dossiers, preparation of JMPR submissions, and Import Tolerance documents for which internal resources did not have the capability or capacity to complete in the timeline needed."
"For 10 years, knoell USA has been my go-to partner for our regulatory submissions. The knoell staff is highly qualified, enthusiastic at work, very well organized and absolutely reliable."
Agrisciences Regulatory Residue Chemistry
"I don’t know what I would do without knoell. We needed someone to review data and coordinate updates in our residue database and help with tasks like creating dossiers and petitions for submission to global regulatory authorities; including IUCLID format for EFSA – something very few consultants have the expertise to do."
Jane Stewart, Team Leader
Crop Protection Consumer Safety
"We needed support for dossier preparation and submission to regulatory authorities and called upon knoell USA to help us with a variety of functions. The team at knoell USA was an invaluable resource, allowing us to focus on other responsibilities and optimize our workload."
Head of Regulatory Data Compliance
Agriculture Seeds & Traits