Services

Services

rapidd™ offers the following integrated services required to go from pre-clinical candidate to phase I regulatory submission. The full range of services are summarised below:

API

  • Toxicology and GMP API Supply
  • API Isotope Labelling
  • Solid State Characterisation

Pre-Clinical Toxicology / Safety Studies

  • Toxicology
  • Safety Pharmacology
  • Bio-analysis
  • Metabolism

Analytical

  • Method Development & Validation
  • API & Drug Product Stability (ICH)

Regulatory

  • Clinical Trial Application (inc. IB and IMPD preparation)
  • USA & Europe

Drug Product

  • Formulation Development
  • Drug Product Manufacture, Packaging, Labelling & Release

Pharmacodynamic Biomarkers

Our typical client base is located in:

  • Europe
  • North America
  • Japan

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