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

At-site Monitoring

Routine at-site monitoring consists of the check of all items stipulated in VICH-GCP such as

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CRF checks

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Data verification

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Adverse events

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Protocol and amendment compliance

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Drug accountability

In-house Monitoring

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Keeping contact to all study participants between the on-site visits is important to be up to date and as a general tool for controlling. In-house monitoring also consists of study file management, sponsor updates etc.