• About Rapidd™
  • Benefits
  • Services
• API
  • Toxicology & GMP Supply
  • Radiolabelling
  • Solid State Characterisation
• Analytical
  • Method Development & Validation
  • API & Drug Product Stability
• Drug Product
  • Formulation Development
  • Product Manufacture, Packaging, Labelling & Release
• Pre-Clinical Toxicology
• Regulatory

Pre-Clinical Toxicology / Safety Studies

Rapidd™ offers world class pre-clinical toxicology and safety assessment in collaboration with a selection of preferred CROs.

A GLP-compliant (ICH S7A) package sufficient for Phase I regulatory submission has been created that will assess undesirable pharmacodynamic effects of a lead candidate on the cardiovascular, respiratory and central nervous systems.

Of course, if you have particular or specific requirements you also have the option of tailoring a bespoke service to suit your needs.

The following areas are covered in Rapidd™:

• Genetic Toxicology
• Toxicology
• Safety Pharmacology
• Formulation Analysis
• Bioanalysis
• Metabolism