Benefits

Benefits

What Offers to Clients:

  • Accelerated development to phase
    • Typically 12 months from lab synthesis to CTA submission
  • Flexible solutions tailored to client requirements
    • Small molecules or peptide
  • Integrated CMC & pre-clinical safety activities
  • Simplified communication
    • Single contract
    • Dedicated programme management support

Benefits of

  • Lead candidate to phase I regulatory submission in 12 months
    • Reduce cash-burn
    • Realise milestones earlier
    • Gain competitive advantage through the acceleration of your drug candidate programme
  • Focus on adding value to your business through your core competences and reduce the effort spent on auditing, coordinating and managing multiple vendors
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