Your products protect crops from pests and disease, optimize growth for maximum productivity, and preserve nature’s bounty and beauty. Either directly or by ripple effect, the development and use of agrochemicals impacts every living creature on our planet. It is important, if expensive, work. Given the $286M average price tag of testing these products for efficacy and safety, it is important to get your products to market quickly. Our world’s food supply, and your bottom line, depend on it.
Being first to market can increase your revenue and deliver a return on the substantial investment in accelerating development, but this demands smooth sailing through the registration process. Even a small bump in the road can derail your program, causing you to miss milestones, fail to meet registration deadlines, and perhaps even lose an entire season of revenue. The ever-changing regulatory landscape only adds to the complexity of the tasks that lie ahead.
Offering a unique combination of scientific capabilities and deep regulatory knowledge across global markets, Charles River can help you grow with expertly designed and executed programs for your agrochemical development and registration.
Our goal at Charles River is to provide clients with a wide range of services that meet their regulatory and scientific needs. Through our global agents and facilities, we can provide clients with more flexibility, experience and expertise in multiple regulatory environments to accelerate the development of their biologic, enabling products to get to market faster.
Article 43 e-Guide
Your resource for plant protection product renewals
Article 43 e-guide
Our REACH e-guide helps you understand requirements, avoid common pitfalls and develop
an effective strategy to register your chemicals.
Our experts are available to answer any questions or discuss a quote.
Supporting your agrochemical registrations
Dynamic Regulatory Knowledge
Our seasoned experts will help you stay one step ahead of the constantly changing regulatory landscape, and dedicate the appropriate resources to ensure compliance. We’ll help you plan studies that not only meet regulatory submission guidelines for the initial target market, but include future-proof data that can be used for submissions in multiple markets create more value for your investment.
Holistic Study Design
Our multidisciplinary toxicologists, environmental scientists and analytical specialists extend your
in-house R&D team with in-depth knowledge of regulatory studies and the know-how to adapt standard designs to meet your specific challenges. An integrated approach ensures each study element achieves its purpose of answering every potential question in the final report.
Deep Scientific Network
You name it, we can do it. From efficacy studies to e-fate, we have the capability and the capacity to execute your studies in a timely fashion. Constant communication and seamless transfer of study data between disciplines and program stages improves data integrity, creates efficiencies, and minimizes risk.
We work within your budget to maximize the outcome for every tactic to eliminate overspending and delays. From the outset of the relationship, we provide a single point of contact who will oversee all aspects of your program and establish regular communications for the optimum use of your time.
Come grow with us
Watch the Video
Your resource for active substance renewals
Designed to inform you of the latest developments in our service portfolio as well as discuss specific technologies and regulatory issues of our industry.
Our Biocides e-guide helps you understand requirements for your biocidal product registration.