Scientific Consulting Company
Consulting firm providing scientific, regulatory and implementation services for chemicals, agrochemicals, biocides, fertilisers/biostimulants, cosmetics, consumer products, medical devices and pharmaceuticals. Core services include regulatory dossier preparation and electronic submission support, hazard/exposure and risk assessment, study monitoring and efficacy trial design, computational toxicology (QSAR, read‑across and grouping), GLP‑compliant archiving, regulatory intelligence and international market‑entry and representation services.
Industries
Nr. of Employees
medium (51-250)
Scientific Consulting Company
Products
registration crop health plant
Scientific and regulatory services helping you register your crop protection products, agrochemicals, and biorationals in Japan, including handling import tolerance applications and MRL setting.
Registration of Crop Health and Plant Protection Products in India
Comprehensive regulatory services for the plant health and nutrition sector in India covering public health pest control, biorationals, biostimulants, and agrochemicals.
UK Agrochemicals & Biorationals Compliance Services
Regulatory services for agrochemicals, biorationals, adjuvants, fertilisers, and biostimulants on the UK market including Great Britain and Northern Ireland.
Biostimulants and Fertilisers Compliance Services
Regulatory and scientific affairs services covering compliance with the European Fertiliser Regulation 2019/1009 for CE-marked products, national and EU registration procedures, and mutual recognition between Member States.
GLP Archiving Services
Complete GLP-compliant archiving concept and central archive service for regulatory needs, including raw data storage under ambient, refrigerated, and deep-frozen conditions with 24/7 monitoring.
Integrated Pest Management (IPM) Regulatory Services
Scientific and regulatory consulting services supporting the integration of Integrated Pest Management (IPM) strategies for plant protection products, biorationals, and agrochemicals within the EU.
registration crop health plant
Scientific and regulatory services helping you register your crop protection products, agrochemicals, and biorationals in Japan, including handling import tolerance applications and MRL setting.
Registration of Crop Health and Plant Protection Products in India
Comprehensive regulatory services for the plant health and nutrition sector in India covering public health pest control, biorationals, biostimulants, and agrochemicals.
UK Agrochemicals & Biorationals Compliance Services
Regulatory services for agrochemicals, biorationals, adjuvants, fertilisers, and biostimulants on the UK market including Great Britain and Northern Ireland.
Biostimulants and Fertilisers Compliance Services
Regulatory and scientific affairs services covering compliance with the European Fertiliser Regulation 2019/1009 for CE-marked products, national and EU registration procedures, and mutual recognition between Member States.
GLP Archiving Services
Complete GLP-compliant archiving concept and central archive service for regulatory needs, including raw data storage under ambient, refrigerated, and deep-frozen conditions with 24/7 monitoring.
Integrated Pest Management (IPM) Regulatory Services
Scientific and regulatory consulting services supporting the integration of Integrated Pest Management (IPM) strategies for plant protection products, biorationals, and agrochemicals within the EU.
Services
Advisory and implementation services covering strategy, dossier preparation and submission, compliance assessment and regulatory representation across chemicals, agrochemicals, biocides, cosmetics, consumer products, medical devices and pharmaceuticals.
Contracted representation and authorised‑representative services to maintain market access and fulfil local regulatory obligations in target jurisdictions.
Contract archive services operated in compliance with GLP principles, supporting long‑term storage, audit readiness and regulatory inspections.
Monitoring, quality oversight and data review for regulatory laboratory and field studies and efficacy trials, including protocol review and report validation.
Application of (Q)SAR, read‑across and other computational methods to support hazard assessment, grouping/prioritisation of metabolites/impurities, data gap filling and non‑animal strategies, with regulatory‑aligned documentation.
Support for MDR/IVDR transition, clinical and biological evaluation, conformity assessment preparation, standards interpretation and device registration processes.
Advisory and implementation services covering strategy, dossier preparation and submission, compliance assessment and regulatory representation across chemicals, agrochemicals, biocides, cosmetics, consumer products, medical devices and pharmaceuticals.
Contracted representation and authorised‑representative services to maintain market access and fulfil local regulatory obligations in target jurisdictions.
Contract archive services operated in compliance with GLP principles, supporting long‑term storage, audit readiness and regulatory inspections.
Monitoring, quality oversight and data review for regulatory laboratory and field studies and efficacy trials, including protocol review and report validation.
Application of (Q)SAR, read‑across and other computational methods to support hazard assessment, grouping/prioritisation of metabolites/impurities, data gap filling and non‑animal strategies, with regulatory‑aligned documentation.
Support for MDR/IVDR transition, clinical and biological evaluation, conformity assessment preparation, standards interpretation and device registration processes.
Expertise Areas
- Regulatory dossier management and electronic submission preparation
- Hazard, exposure and environmental fate modelling
- Computational toxicology, (Q)SAR and read‑across/grouping approaches
- New Approach Methodologies (in vitro and in silico) and integrated testing strategies
Key Technologies
- Rule‑based and statistics‑based (Q)SAR models
- Read‑across and analogue grouping methodologies
- OECD QSAR toolbox and complementary in silico tools
- IUCLID dataset management and API integration
News & Updates
Guidance on ECHA account features for linking substances, saving searches and receiving procedural update alerts; includes advice on accessing IUCLID and other ECHA tools.
Summary of timelines for a harmonised chemical risk assessment platform and participation in stakeholder expert groups and platform testing.
Summary of IUCLID 6 new features, including single sign‑on, PostgreSQL support, public API for system integration, improved import/export and dossier comparison features.
Guidance and ePoster on grouping, read‑across and prioritisation methods for hazard and risk assessment of active substance metabolites.
Multimedia guidance on applications of in silico toxicology and ecotoxicology in regulatory assessment.
Video guidance on occupational exposure assessment approaches for plant protection products.
Guidance on ECHA account features for linking substances, saving searches and receiving procedural update alerts; includes advice on accessing IUCLID and other ECHA tools.
Summary of timelines for a harmonised chemical risk assessment platform and participation in stakeholder expert groups and platform testing.
Summary of IUCLID 6 new features, including single sign‑on, PostgreSQL support, public API for system integration, improved import/export and dossier comparison features.
Guidance and ePoster on grouping, read‑across and prioritisation methods for hazard and risk assessment of active substance metabolites.
Multimedia guidance on applications of in silico toxicology and ecotoxicology in regulatory assessment.
Video guidance on occupational exposure assessment approaches for plant protection products.