Quality Assurance & Regulatory Support for Live Biotherapeutics

  • 3 Qualified Persons (QP)
  • Fully compliant with European Clinical trials Directive 2001/20/EC, ICH and applicable FDA standards
  • Licensed for cGMP manufacture in Sweden and the UK
  • Support customers with their CMC filings
  • QP release & shipment to clinical trial sites

Other Microbiota Services...

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