OUR SERVICES
Trainings
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HIPAA/Patient Privacy Laws
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Monitoring
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Study Coordinator Responsibilities
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Clinical Investigator Responsibilities
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Clinical Research Consultation
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New, Experienced or Non-Experienced in Clinical Research
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On-Site Near Your Location (Local/Regional)
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On-Going Training (Initial, Refresher)
Classes Focus On:
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The Knowledge of Identifying, and Maintaining Compliance
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Field-Proven Specific Skills and Techniques
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How to become an "A" Ranking site
Any Organization
including Sponsors:
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Clinical Investigators
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Contract Research Organizations (CROs)
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Customized Classes
Monitor
Our training has been created for developing the monitoring, coordinating, and investigating tools and techniques that will systemically design, establish, control, evaluate and continually improve processes in clinical research trials for superior performance excellence.
Clinical Trials
Skill-based training philosophy allows the delivery of practical information for your organization to conduct a clinical research trial in a safe, compliant, and professional manner.
GCP/HIPAA
Knowledge of Identifying and Maintaining Compliance, Patient/Subject Safety, and Privacy.
Knowledge of and compliance with all Applicable Code of Federal Regulations (CFR), and Good Clinical Practice (GCP) References (ICH Guidelines when applicable).
