At GenEvolutioN, we provide in-vitro testing solutions for a wide range of industries, including pharmaceuticals, cosmetics, medical devices, food, agro-science, and chemicals. Our expertise ensures compliance with global regulations and supports innovation in each sector.

GenEvolutioN stands out as a fully independent Contract Research Organization (CRO) specializing in in-vitro genetic toxicology and toxicology expertise. Our key differentiators include:

• Cutting-Edge Innovation → We leverage advanced human cell and reconstructed tissue models alongside state-of-the-art analytical technologies to predict cancer risks and anticipate future challenges.
• GLP-Accredited & Regulatory Expertise → Our laboratories are GLP-compliant, inspected by ANSM (French Health Authority) and COFRAC-certified, ensuring full alignment with OECD, FDA, EMA, and REACH regulatory requirements.
• Tailored Solutions & Custom Study Designs → Unlike many CROs, we offer personalized testing strategies, miniaturized assays, and next-generation sequencing approaches to deliver precise, high-throughput results.
• Commitment to Non-Animal Testing → We focus on alternative, ethical, and predictive in-vitro methodologies to provide reliable safety assessments while reducing animal testing dependency.
• Strong Scientific & Business Expertise → Founded by renowned industry experts from Sanofi & Covance, our team combines decades of experience in toxicology, regulatory sciences, and business development.

At GenEvolutioN, we go beyond testing—we provide strategic insights, regulatory guidance, and innovation-driven solutions to help our clients accelerate product development while ensuring safety and compliance.

Collaborating with GenEvolutioN is seamless and tailored to your specific needs. Whether you’re a pharmaceutical company, cosmetics manufacturer, medical device developer, or chemical producer, we offer a structured approach to partnership:

1. Define Your Needs → Contact us to discuss your project requirements, whether it’s genotoxicity screening, regulatory toxicology studies, or custom R&D solutions.
2. Customized Study Proposal → Our experts will assess your objectives, recommend the most relevant testing strategies, and provide a detailed study outline aligned with GLP and regulatory standards.
3. Project Execution & Real-Time Collaboration → We ensure transparent project management, with regular updates, direct access to our scientific team, and a collaborative approach to data interpretation and regulatory reporting.
4. Regulatory Support & Consulting → Beyond testing, we assist in regulatory submissions, risk assessments, and compliance strategies to help navigate complex industry regulations.
5. Long-Term Partnership & Innovation → We support ongoing R&D, provide knowledge-sharing opportunities, and explore innovative methodologies, such as AI-driven toxicology solutions for future regulatory trends.

Interested in collaborating? Contact us today to explore how GenEvolutioN can support your projects with cutting-edge toxicology expertise and regulatory insights.