Our Services

At Toxiqua, we provide expert study monitoring and coordination services to ensure the successful execution of outsourced toxicology projects. With years of experience managing complex studies, we act as your trusted partner to oversee every stage of the process—from design and implementation to reporting and regulatory compliance.

• Oversight of Good Laboratory Practice (GLP) studies.

• Coordination of timelines, budgets, and deliverables.

• Regular updates and communication with Contract Research Organizations (CROs) to ensure progress aligns with your objectives.

• Quality control and review of study data to meet international regulatory standards, including OECD guidelines and EU regulations.

Navigating regulatory frameworks can be challenging. Toxiqua offers specialist representation at ECHA’s Risk Assessment Committee (RAC), Biocidal Products Committee (BPR WG), and other regulatory authority meetings. Our team has the expertise to advocate on your behalf, ensuring your interests are effectively communicated.

• Preparation of technical dossiers and argumentation.

• Advocacy for classification, labeling, and authorization strategies.

• Liaison with regulatory bodies to clarify requirements and expectations.

• Expert support during discussions and negotiations.

Toxiqua specializes in developing robust classification and labeling (C&L) strategies that align with global standards such as CLP Regulation and GHS. We help clients present persuasive technical positions and advocacy approaches to secure favorable regulatory outcomes.

• Detailed hazard assessment and classification justification.

• Preparation of technical arguments for RAC submissions.

• Risk-based labeling recommendations tailored to product use.

• Stakeholder communication and negotiation.

Choosing the right Contract Research Organization (CRO) is critical to the success of your toxicology projects. At Toxiqua, we leverage our industry knowledge to provide unbiased CRO selection and recommendations that suit your specific needs.

• Identification of CROs with expertise in your field.

• Evaluation of capabilities, compliance history, and costs.

• Negotiation of contracts and timelines.

• Ongoing support to optimize CRO performance.

Toxiqua provides tailored testing strategy development to meet the unique requirements of your regulatory and scientific needs. Our team designs efficient and cost-effective testing programs that comply with international standards such as REACH, BPR, and PPP.

• Identification of key data requirements.

• Prioritization of tests to address regulatory gaps.

• Optimization of animal testing reduction strategies, including New Approach Methodologies (NAMs).

• Comprehensive risk assessment frameworks.

Toxiqua’s data gap analysis services help clients identify missing information and develop plans to fill those gaps efficiently.

• Systematic review of existing datasets.

• Identification of missing or insufficient data.

• Recommendations for new studies or alternative approaches, such as QSAR models and read-across methods.

• Preparation of regulatory-compliant documentation.

Toxiqua is a trusted partner for preparing high-quality OECD and IUCLID dossiers for compliance with Plant Protection Products (PPP), Biocidal Product Regulation (BPR), and REACH. Our meticulous approach ensures your submissions meet all regulatory requirements.

• Comprehensive dossier preparation and data entry in IUCLID.

• Alignment with OECD guidelines and EU regulatory frameworks.

• Management of dossier updates and amendments.

• Expert advice on submission strategies.

Toxiqua employs advanced QSAR (Quantitative Structure-Activity Relationship) models, New Approach Methodologies (NAMs), and read-across techniques to reduce reliance on animal testing while ensuring robust safety assessments.

• Application of computational toxicology tools.

• Development of read-across justifications in line with regulatory standards.

• Implementation of NAMs to meet 3Rs (Replacement, Reduction, Refinement) principles.

• Integration of QSAR and in vitro data for comprehensive hazard assessments.

Toxiqua provides fast, reliable answers to your most pressing regulatory questions and queries. With deep expertise in toxicology and global regulations, we offer practical guidance to help you navigate complex compliance requirements.

• Clarification of regulatory guidelines for REACH, BPR, and other frameworks.

• Interpretation of technical requirements.

• Strategic advice for submissions and negotiations.

• Rapid response to urgent compliance issues.

Toxiqua provides deep expertise in Endocrine Disruption to address regulatory needs and questions.

EU ED assessments as outlined in the 2018 ECHA-EFSA guidance on the identification of endocrine disruptors and encompasses human health and the environment.

The principles here are also applicable to how we will assess under CLP for classification based on the legislative wording and the CLP guidance document.