Study Design
  • The most flexible protocol on the market supports the widest variety of study designs
  • Support for General Toxicology, Reproductive Toxicology and Safety Pharmacology
  • Highest quality data management by averting data duplication or redundancy
  • Accounts for all the required reviews and approvals and amendments
  • Scheduling events to all animals, individual animals, groups, sex, sub-group or litter
  • Scheduling of daily in-vivo measurements, sample collections, sample analyses, necropsy activities and pathology requirements
  • Full GLP and OECD compliance