The "Practical Implementation of GCP in Veterinary Field Studies" conference has been added to ResearchAndMarkets.com's offering.

This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with GCP as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP.

The meeting will address a typical case study where a practical approach will be made to setting up, running and monitoring clinical trials followed by an audit of these studies to satisfy the stringent requirements seen in Europe.

Standard documentation utilised for recording data, performing audits and a typical protocol will be supplied for use in the company attendees' own laboratories.

Key Takeaways:

  • Understand the regulatory requirements and study design
  • Know how to design protocols and apply them
  • Take away practical advice on how to set up clinical trials
  • Clarify the pharmacovigilance requirements
  • Gain a better understanding of data handling and appropriate' statistics
  • Discover how to produce the final report
  • Assure quality in laboratory field studies

Agenda

Programme Day One

  • The Regulatory Requirements and Study Design
  • Protocol Design and Application
  • Setting up Clinical Trials - A Practical Case Study
  • Pharmacovigilance Requirements and Considerations

Programme Day Two

  • Data Handling and Appropriate' Statistics
  • Producing the Final Report
  • Assuring Quality in Laboratory and Field Studies

For more information about this conference visit https://www.researchandmarkets.com/research/cd26fj/2_day_seminar?w=4