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Monitoring

The monitoring is a major part and a key for sucessful studies. Therefore we  guarantee that monitoring will only be done by qualified veterinarians experienced in conducting clinical trials.

Lean more about

Site Monitoring
  • Routine at-site monitoring consists of the check of all items stipulated in VICH-GCP such as
  • CRF checks
  • Data verification
  • Pharmacovigilance
  • Protocol and amendment compliance
  • Drug accountability

In-house Monitoring
  • contacts and correspondence
  • study management
  • sponsor updates

ickstattstr. 5 I 80469 munich I germany I tel +49 (0) 89 23 000 123 I fax +49 (0) 89 23 076 763
info@vet-research.com I www.vet-research.com