#safetyassessment

𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐚𝐠𝐞𝐧𝐜𝐢𝐞𝐬 𝐦𝐚𝐲 𝐫𝐞𝐪𝐮𝐢𝐫𝐞 𝐉𝐮𝐯𝐞𝐧𝐢𝐥𝐞 𝐀𝐧𝐢𝐦𝐚𝐥 𝐓𝐨𝐱𝐢𝐜𝐨𝐥𝐨𝐠𝐲 (𝐉𝐀𝐒) 𝐬𝐭𝐮𝐝𝐢𝐞𝐬 𝐛𝐞𝐟𝐨𝐫𝐞 𝐢𝐧𝐢𝐭𝐢𝐚𝐭𝐢𝐧𝐠 𝐩𝐚𝐞𝐝𝐢𝐚𝐭𝐫𝐢𝐜 𝐜𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐭𝐫𝐢𝐚𝐥𝐬—𝐞𝐬𝐩𝐞𝐜𝐢𝐚𝐥𝐥𝐲 𝐰𝐡𝐞𝐧 𝐝𝐞𝐯𝐞𝐥𝐨𝐩𝐦𝐞𝐧𝐭𝐚𝐥 𝐭𝐨𝐱𝐢𝐜𝐢𝐭𝐢𝐞𝐬 𝐚𝐫𝐞 𝐚𝐧𝐭𝐢𝐜𝐢𝐩𝐚𝐭𝐞𝐝. When toxicities can’t be measured in early human studies, these preclinical safety assessments fill in the gaps. Each study for this is uniquely designed—tailored to your compound, patient age group, and organ systems of concern like neurological, reproductive, or skeletal. Our team has supported global sponsors with customized, GLP-compliant juvenile toxicity studies—combining regulatory expertise with a deep understanding of pediatric development. ✅ Over 20+ juvenile rodent studies completed successfully across varied dosing routes ✅ Case-by-case protocol planning ✅ Global registration alignment Looking for a CRO that speaks both science and strategy? Let’s design your next juvenile toxicology study together. Connect with our experts – [email protected]

We understand the critical role that comprehensive safety evaluation plays in drug development. Our team of experts along with advanced technologies and specialized equipment enables us to conduct precise and reliable studies. We are committed to providing exceptional services to our clients. Partner with us for comprehensive safety assessment services that keep your projects on track and risk-free. 🤝 To know more, click on the link 👉 https://lnkd.in/g6eBPfa2

𝐒𝐭𝐫𝐞𝐚𝐦𝐥𝐢𝐧𝐞𝐝 𝐃𝐫𝐮𝐠 𝐃𝐞𝐯𝐞𝐥𝐨𝐩𝐦𝐞𝐧𝐭 𝐰𝐢𝐭𝐡 𝐄𝐮𝐫𝐨𝐟𝐢𝐧𝐬 𝐀𝐝𝐯𝐢𝐧𝐮𝐬! We ensure efficient operations, accelerated timelines, enhanced communication and cost-effective solutions. Partner with us to experience the benefits of unified CMC and Pharmtox framework.

Discover our cutting-edge In Vitro Regulatory Toxicology Services! 🔬 With a wealth of experience and state-of-the-art facility, we offer comprehensive in vitro safety assessment services for pharmaceuticals, medical devices, agrochemicals, industrial chemicals and food additives. Trust us for top-notch solutions in ensuring product safety and regulatory compliance. Follow us for latest updates

Unravel the complexities of nitrosamine genotoxicity with Eurofins Advinus. To provide you with a deeper understanding of potential risks, we offer a comprehensive package that includes - 🧬 Genetic toxicology studies 🧬 Comet assay 🧬 PigA mutation assay Contact us to discuss your project requirements - [email protected]

We can assist you with the Environmental Risk Assessment (ERA) of your medicinal products in a tiered approach as per EMA Guideline on the Environmental Risk Assessment of Medicinal Products for Human Use. We conduct Phase I assessment, which includes the calculation of the Predicted Environmental Concentration (PECSW), and recommend studies to be performed in the Phase II Tier A assessment. For the PBT/vPvB assessment, we can determine the octanol/water partition coefficient. Based on the results, we suggest any additional studies that may be necessary. Our GLP laboratories can conduct all required studies for both ERA Phase II Tier A and Tier B, as well as the studies needed for PBT/vPvB assessments. Contact us to discuss your project requirements - [email protected]

📢 Our team is participating at LASACON 2024. We look forward to meeting with you at the event in Mumbai on 📆 29-30 November, 2024. We are committed to work with our community to make research better and safer. If you would like to schedule a meeting with us during the conference, write to us at 📧 [email protected] To know more about our services, click on the link - www.advinus.com