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Callisto Regulatory Consulting Ltd

Callisto Regulatory Consulting has extensive experience of human, herbal and veterinary medicines, medical devices, biocides, borderline products and food supplements. From this experience we are able to provide a range of regulatory, pharmacovigilance and technical services that are tailored to meet our client’s specific needs. These include:

  • 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 including batch release activities
  • GMP, GDP and PV audits
  • Training in all areas
  • Readability testing of labels and leaflets.

For more information please follow the link “Callisto Regulatory Consulting”.

callisto regulatory consulting

Batch release of human & veterinary medicines to market, Qualified Person (QP) services & pharmaceutical auditing from Elara Pharmaservices. MHRA & VMD approved.


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