SynTech Research Group delivers global regulatory solutions.
SynTech Research offers unparalleled expertise in navigating complex global regulatory landscapes. Our teams combine decades of experience with deep knowledge of national and international requirements, ensuring your products meet compliance standards in an efficient and agile manner. We provide strategic guidance across all stages, from regulatory planning and data gap analysis to dossier preparation and submission, supported by robust confidentiality frameworks and coordinated taskforces for multi-stakeholder alignment. With specialists worldwide, we harmonize processes to deliver submission-ready documentation that accelerates registration and market access. By integrating scientific rigor with regulatory precision, SynTech helps you move confidently from development to approval.
Full range of services for the registration of agrochemical products: from herbicides to fungicides and insecticides, covering both simple active substances and complex formulations. Our support includes data gap analysis, risk assessment, dossier preparation, and national submissions.
Encompassing all biological actives classified as Biostimulants and Biocontrol, including semiochemicals, natural substances (botanicals, biochemicals, microbial extracts, minerals,…) and microorganisms.
In addition to the preparation of dossiers for biocidal active substances and products, we constantly monitor the developments of the regulatory affairs assuring an exhaustive fulfilment of your obligations as a producer.
Advisory from the early stages of formulation to the final placing of the product on the market.
Dossiers for the environmental risk assessment of human as well as veterinary medicines.
Specialized in the area of ecotoxicology, environmental fate, and behavior as well as physico-chemical properties of industrial chemicals. Additional areas are covered through the well-established and reliable co-operation with partners.
We redefine regulatory support through agility and precision. We bespoke the strategy and the team for each project, to optimize costs and timelines. Parting away from large, fragmented structures, our consultancy teams are small, specialized, and fully dedicated to your projects, ensuring fast decision-making, streamlined communication, and commitment to your timelines. Our global footprint brings together professionals from over 60 countries, offering a unique advantage: multilingual capabilities that make interactions with clients and local authorities effortless. Combined with decades of regulatory expertise and a commitment to efficiency, SynTech delivers submission-ready documentation and strategic guidance that accelerate your path to market.
Our consultancy delivers end-to-end regulatory expertise, ensuring compliance and efficiency at every stage of your product’s journey. From study oversight to dossier preparation and regional submissions, we provide specialized support tailored to global and national requirements.
Following a comprehensive approach to ensure your project meets all regulatory requirements efficiently and transparently. It begins with project evaluation, where we review your objectives, product profile, and target markets to define the regulatory scope and strategy. Next, we provide tailored guidance on compliance pathways, including identifying applicable regulations, timelines, and dossier requirements. To safeguard confidentiality and collaboration, we establish NDAs and, when needed, coordinate multi-stakeholder taskforces to streamline communication and decision-making. We can contract and monitor all needed studies to make sure they comply with multiple countries (or regions) requirements to avoid having to repeat studies. Throughout the process, we manage documentation, data integrity, and alignment with global standards, ensuring every step supports a successful registration outcome. Finally, we deliver submission-ready materials, including regulatory summaries and supporting reports, designed for direct inclusion in registration dossiers or internal assessments.
SynTech Research combines worldwide coverage with extensive national experience, ensuring seamless communication with clients and regulatory authorities in every region. Our network spans more than 60 countries, supported by experts who proficient in a diversity of languages, cultural frameworks, and regulatory frameworks. This approach accelerates approvals, reduces complexity, and guarantees compliance with regional requirements while maintaining harmonized standards across markets. Wherever your product needs to go, SynTech ensures smooth navigation from development to registration.
Regulatory services at SynTech Research Group are built on strict adherence to international standards, ensuring accuracy, transparency, and trust in every submission. We operate under globally recognized frameworks, region-specific guidelines, supported by rigorous internal quality assurance audits. Our processes guarantee that all documentation, data summaries, and assessments meet the highest compliance benchmarks, accepted by regulatory authorities worldwide. With a strong commitment to scientific integrity, confidentiality, and ethical practices, we deliver submission-ready dossiers and supporting reports that enable reliable decision-making and successful product registration across diverse markets.
Accelerate your product development with our expert regulatory consultancy, designed to deliver robust, validated dossiers supports confident market claims. Streamline registration processes and enhance credibility with regulators and stakeholders, ensuring faster time-to-market and stronger competitive positioning.
For general enquiries email info@syntechresearch.com or please use the contact form below