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Staphyt

Unclaimed
Contract Research OrganizationsServicesstaphyt.comInchy-en-Artois, FranceUpdated

Staphyt provides field research, laboratory studies, and regulatory consulting to support clients throughout product development.

Overview

Staphyt is an international service provider and regulatory affairs consultant serving the agroscience, biocide, chemical, and pharmaceutical sectors. Its teams of scientists, agronomists, and regulatory experts support clients throughout product development, from field research and laboratory studies to regulatory strategy, registration, and commercialization. Staphyt combines technical expertise and tailored services to help clients develop products and varieties and contribute to more sustainable agriculture.

Mission statement

Acting together to feed the world sustainably.

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What we offer

Field services

Service

Helps agricultural clients evaluate products and varieties, generate useful field data, and advance development and market approval.

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Laboratory services

Service

Provides specialist laboratory testing and analysis to characterise substances and assess their environmental impact and fate.

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Regulatory Affairs and Consultancy

Service

Helps clients plan regulatory pathways, address data requirements, and progress products toward registration and market launch.

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BioTeam services

Service

Develops biological products with coordinated testing, laboratory analysis and regulatory support from early development through registration.

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Phytnet

Gives clients secure access to study information and a direct, efficient way to communicate with Staphyt project teams.

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More information about our offering

Field services

Staphyt provides customised agricultural research through officially recognised field trial stations and partner sites. Field agronomists, project managers and scientists test products and varieties to assess performance, efficacy and safety. Services include efficacy and positioning trials, residue studies, fertilisation trials, seed care and breeding, and GMO and special-project studies. Staphyt designs studies around client requirements and supports trial programmes from early product development through launch, working with its Regulatory Affairs department where needed. Study capabilities include field, semi-field, laboratory and controlled-environment trials, as well as research, screening, registration and demonstration work.

  • Generate Data For Approval Dossiers
    Produce experimental results and reports for approval documentation and registration submissions using applicable regional methods.
  • Access Recognised Trial Sites
    Use field stations and partner locations to conduct agricultural research across multiple regions and production conditions.
  • Adapt Trials To Study Needs
    Receive study designs, protocols, sites and testing conditions matched to product, crop and research requirements.
  • Evaluate Product Performance And Positioning
    Generate field evidence on product efficacy, crop safety, use patterns and positioning to inform research and development decisions.
  • Measure Residues And Exposure
    Obtain field data on residues in crops, stored foods, soil and beehive products, as well as human exposure and product drift.
  • Assess Plant Nutrition Products
    Evaluate fertilisers and biostimulants through measurements of plant performance, nutrient use, soil-related outcomes and treatment effects.
  • Evaluate Varieties And Seed Treatments
    Assess varieties, seed production and seed treatments through field and nursery trials to support selection, breeding and development.
  • Study GMO Performance And Pest Responses
    Conduct accredited studies of GMO cultivars, target-organism control, pest susceptibility, population dynamics and resistance-related outcomes.
  • Match Trial Setups To Study Needs
    Choose suitable trial scales, environments, equipment and monitoring methods, including laboratory coordination, satellite positioning and drone measurements.
  • Run Trials And Demonstrate Products
    Use precision sowing and harvesting for trials, and field platforms to demonstrate products and varieties to relevant audiences.
  • Share Study Information Securely
    Use a secure digital platform to exchange study information and access trial records and reports.
  • Assess Nematode And Residual Effects
    Evaluate plant and cultivar responses to nematodes and examine residual treatment effects in relation to soil conditions.

Laboratory services

Staphyt provides laboratory services to test, screen and evaluate products using specialist expertise and equipment. Its laboratories conduct GLP analyses to characterise substances and assess their impact and fate in the environment. Services include analytical method development and validation for pure substances and UVCB products, physicochemical analyses, five-batch analyses, storage stability, biodegradability, bioaccumulation, environmental fate, and terrestrial and aquatic ecotoxicology studies.

  • Test And Evaluate Products
    Use laboratory testing, screening and evaluation supported by specialist expertise and laboratory equipment.
  • Characterise Substances Under GLP
    Obtain GLP laboratory analyses to characterise substances, including physicochemical and five-batch analyses.
  • Develop And Validate Analytical Methods
    Develop and validate analytical methods for pure substances and UVCB products.
  • Assess Environmental Fate
    Study the fate of substances in the environment as part of GLP laboratory analyses.
  • Assess Terrestrial And Aquatic Ecotoxicity
    Conduct terrestrial and aquatic ecotoxicology studies to assess the environmental impact of substances.
  • Assess Environmental Substance Properties
    Conduct studies to assess the biodegradability and bioaccumulation of substances.
  • Assess Storage Stability
    Conduct laboratory studies to assess product storage stability.

Regulatory Affairs and Consultancy

Staphyt’s regulatory experts help clients define regulatory strategies and guide products, substances and varieties through registration and commercialisation. Services include data gap audits, go-to-market strategy and project budget assessment, contact with regulatory authorities, follow-up of GEP and GLP studies, risk assessments, and drafting and submission of approval and registration dossiers. Staphyt operates internationally in the agroscience, biocide, chemical and pharmaceutical sectors.

  • Plan Regulatory Pathways
    Develop regulatory and market-entry plans to guide products toward registration and commercialisation.
  • Prepare Registration Dossiers
    Receive support in drafting and submitting dossiers for product approval and registration.
  • Identify Data Needs
    Assess existing data and identify gaps to clarify what a project requires for its regulatory pathway.
  • Engage Regulatory Authorities
    Communicate with authorities and consider their expectations and data requirements when planning regulatory work.
  • Assess Product Risks
    Evaluate risks to people, non-target organisms and the environment to support product registration.
  • Coordinate Study Follow-Up
    Support the follow-up of GEP and GLP studies as part of the regulatory project.
  • Estimate Project Budget
    Assess the potential budget associated with a project as part of its planning.

BioTeam services

BioTeam supports the development of biopesticides and biostimulants, including products based on natural extracts, microbial agents and semiochemicals. Its agronomists, scientists and regulatory experts combine controlled-condition and field trials, GLP laboratory analyses and regulatory consultancy. Support can begin in the early development stages and extend through efficacy testing, risk assessment, regulatory strategy and preparation and submission of registration dossiers.

  • Plan Regulatory Strategy And Submissions
    Get support with market strategy, data needs, authority engagement, study follow-up and preparation and submission of approval or registration dossiers.
  • Evaluate Products In Field Conditions
    Generate field evidence on biological product efficacy and positioning using protocols adapted to the product, crop, application and targeted claims.
  • Characterise Substances Under GLP
    Obtain GLP laboratory data on substance properties, stability, environmental fate and ecotoxicology, with analytical methods developed and validated for pure substances and UVCB products.
  • Characterise Biological Products
    Use controlled-condition trials to investigate product characteristics, mode of action and performance in relevant environments.
  • Assess Product Risks
    Evaluate risks to humans, non-target organisms and the environment to support product characterisation and regulatory work.
  • Coordinate Development Projects
    Work with one project manager who coordinates specialists and supports the project from early development through regulatory activities.
  • Screen Substances And Products
    Assess biological substances and products for abiotic stress resistance, elicitor effects, in vitro efficacy, compatibility and dose.
  • Position Products In IPM Programs
    Evaluate how a biological product fits within an optimised IPM programme, with or without conventional products as appropriate.

Phytnet

Phytnet is a platform developed by Staphyt’s technical and IT teams for managing projects and enabling secure communication between clients and Staphyt teams. It provides access to study data and records, including trial photos, planning, plot locations and study reports. Phytnet is currently available for studies managed in Europe.

  • Access Study Information Around The Clock
    Clients can securely access study data and studies at any time through the platform.
  • Communicate Directly With Project Managers
    The platform supports client communication with Staphyt teams and provides a direct channel to project managers responsible for study documents.
  • Review Study Results Transparently
    Clients can use the platform to support transparency around study results.
  • Transfer Study Information Quickly
    The platform facilitates information exchanges and helps clients receive study-related information quickly.
  • Review Study Records And Trial Details
    Review study history through trial photos, planning, plot locations and study reports.
  • Use A Personalised Interface
    Clients use a personalised interface designed to be simple and quick to use.

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