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Compliance Training Webinar
How to Write an ICH-Compliant Clinical Study Report
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This Clinical Study Report webinar/training is designed to provide guidance for producing such a document, included are the outline format, concepts, guidance for text, and guidance for the appendices. Price : $299.00  
Instructor Robert S Hoop Recorded Webinar
What are the Investigator responsibilities in Research Involving Human Subjects: The International Conference on Harmonization (ICH) position
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This Clinical research training will provide invaluable assistance to investigators and their staff in the regulatory / legal responsibilities and also the ethical considerations in pharmaceutical product research involving human subjects. Price : $299.00  
Instructor Charles H Pierce Recorded Webinar
FDA?s Clinical Trials Audit procedures companies should conduct as part of its monitoring program
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This Clinical Trial Audit webinar / training is designed to provide information on the importance of having an audit plan in place for clinical trials to be submitted to the FDA. Development of an independent audits/data verification and compliance monito Price : $299.00  
Instructor Carol Owen Recorded Webinar
How to Create and Understand A Statistical Analysis Plan for A Clinical Study
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This statistical analytical plan webinar training will guide the attendees how to create a SAP and showcase the essential elements of it and how to create as per the expectations of regulatory bodies. Price : $299.00  
Instructor Robert S Hoop Recorded Webinar
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