Welcome to Callisto Regulatory Consulting

Callisto Regulatory Consulting work across UK, Europe, and the rest of the world for a range of global, mid-sized and small pharmaceutical, healthcare and veterinary medicines companies.

Our team has extensive experience of human, veterinary and herbal medicines, medical devices, borderline products, biocides and food supplements over most dosage forms and can offer the following services:

  • Preparation and submission of regulatory dossiers
  • Full technical support to manufacturers, including technical transfer, manufacturing support and analytical trouble-shooting
  • Complete Pharmacovigilance Services including QPPV appointment
  • Support with development projects
  • QP and RP services include batch release activities
  • GMP, GDP, GLP and PV audits
  • GxP training
  • Readability testing of labels and leaflets.

Callisto Consulting are part of a group of companies that can provide complete services to the pharmaceutical industry including regulatory applications, pharmacovigilance, QP batch release, manufacturing and API site audits. We can also provide assistance with product development and technical transfer projects.

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Complete range of regulatory services. Extensive experience of human and veterinary medicines, herbal medicines, borderline products, food supplements and cosmetics.

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