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On board, our core team comprises specialists in every aspect of the Development process:
  • Regulatory Affairs (EU/US)
  • Preclinical Studies
  • Toxicology 
  • Manufacturing (CMC) for recombinant proteins, antibodies, chemicals, peptides
  • Analytical Methods (Development & Validation)
  • Clinical Development (EU/US)
  • Industrialisation

Having worked both in Start-ups and big Pharmas, our team members are aware of the needs of the industry and can adapt themselves to the demands of the project. From Synthesis and Cloning to Marketing Authorization, we commit ourselves to quality solutions every step of the way.