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The key trainer in KLR is a qualified clinician with at least 10 years’ experience in medical practice, and with years of experiences in global pharmaceutical industry. She has worked on clinical trials and regulatory affairs in China for more than 12 years, and is familiar with the regulations of ICH. She is the CFDA GCP and Monitoring trainer, and has trained more than 20, 000 clinical physicians and more the 3000 monitors and Project Managers from a variety of pharmaceutical companies. KLR can provide the clients with: ※ICH GCP and Chinese GCP guidelines and Chinese regulations ※Clinical trial and regulatory guidance and training on GCP ※Trainings for monitors of different levels ※Trainings for clinical trials of different period ※Trainings for different roles in clinical trials ※Site monitoring and project management ※Specific team training for pharmaceutical company ※Specific SOP system and related trainings
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