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KAI provides on-site, customized training designed to improve employee performance
and overall regulatory compliance. We develop and adapt training courses to meet
your specific compliance needs in:
- Fundamentals of GCP
- Effective Monitoring and Auditing Techniques
- FDA Inspection Readiness
Our on-site trainers provide you with the most useful and up-to-date information
available on regulatory matters as they apply to clinical trials. They have:
- Clinical Research subject matter expertise
- Extensive clinical research experience
- Proven track record of successful training within the
clinical research industry
KAI aligns targeted GCP compliance training to your company's strategy.
For more information, please contact us at GCP_QA@kai-research.com.