Practical Implementation of GCP in Veterinary Field Studies 2025 in London, Great Britain

This two-day course, Practical Implementation of GCP in Veterinary Field Studies, will provide a comprehensive overview and offer practical approaches to designing, designing and conducting veterinary clinical trials in accordance with VICH Good Clinical Practice (GCP) principles and other regulatory guidelines.

The program will cover the responsibilities of all teaching roles, required documentation, data processing processes and statistical analysis. The sessions will also examine the appropriate quality standards that must be applied to warrant data acceptable to regulators in the EU and US.

Delegates are expected to work through a range of challenging case studies that will help consolidate learning. There will also be an opportunity to discuss this with experts who have significant experience in this field.

Benefits of visiting:

• Understand regulatory requirements and study design
• Know how to write compatible protocols
• Get practical advice on organizing clinical trials.
• Learn how to practically conduct and manage clinical trials
• Clarify specific aspects of clinical trials
• Gain a better understanding of data and “relevant” statistics
• Learn how to write a final research report (FSR)
• Ensure the quality of clinical studies

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