Reduce early, or late stage, set backs in the registration procedure
Reduce early, or late stage, set backs in the registration procedure by anticipating questions from regulators
This course is aimed at anyone who comes into contact with PK/PD data but does not require specialist knowledge in the field. No previous knowledge of PK/ PD is assumed. The course is designed to give an overview of the field without the equations. It will be of particular benefit to professionals working in:
• Development
• Preclinical
• Phase I
• Licensing
• Clinical Operations
• Regulatory affairs
• Data management
• Drug safety
• Clinical pharmacology
• Registration
"Really Useful, dynamic course"
"Concepts well explained"
"Excellent course"
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"Effective training to enable productive collaboration with PK team and validation/review of clinical trial documents" - MD, Head of Therapeutic Strategic Unit, Sanofi-Aventis |
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