Pharmaceuticals
Toxway: Empowering Pharmaceutical Excellence with Safety and Compliance
Toxway is committed to ensuring the highest standards in pharmaceutical product safety through our specialized toxicology and safety assessment services. Our expert team is dedicated to helping you navigate complex regulatory requirements and optimize product safety. Discover our comprehensive range of services tailored to the pharmaceutical industry.
Our Sevices
Health-Based Exposure (HBEL) Limits
Toxicological Risk Assessments
Paper-Based Safety Justification of Drug Substance/Impurity (ICH Q3A & Q3B)
See MorePaper-Based Safety Justification of Elements (ICH Q3D)
See MoreGenotoxicity/Mutagenicity Assessment (ICH M7)
See MoreStudy-Based Safety Justification for Drug Substance/Impurity
See MoreNitrosamine Safety Assessment
See MoreOther Services
Molecular Categorization
See MoreMSDS Authoring (REACH & OSHA)
See MoreE&L Toxicological Risk Assessment
See MoreF-Value Calculations
See MoreExcipients Safety Assessment
See MoreNon-Clinical Study Waivers
See MoreGLP CRO Selection & Study Monitoring
See MoreCRO Qualification for Preclinical Studies
See MoreResearch Publication and White Paper Support Services
See MoreChoose Toxway for Pharmaceuticals to ensure your products meet global safety and quality standards with expert precision. Our regulatory expertise spans ICH, USFDA, EMEA, REACH, and OSHA, offering comprehensive guidance for seamless compliance and market access. We deliver tailored solutions to address your unique project demands, with a personalized and flexible approach to adapt to evolving needs. Backed by a team of seasoned toxicologists and industry experts, we bring deep knowledge, a proven track record, and reliable solutions to every project. Trust Toxway as your dedicated partner in achieving pharmaceutical excellence and advancing your success.