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Quick Links
Additional Information
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Courses offered
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Instructor Led Courses

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Pharmaceutical development from Discovery to Marketing
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Good Manufacturing Practices
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Good Laboratory Practices
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Clinical Research Process
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Good Clinical Practices

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Patient Recruitment Strategies
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Medical Terminology
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Informed Consent Development
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Anatomy and Physiology
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Government regulations and Guidelines in Clinical Research including International Conference on Harmonization, European Clinical Trial Directive, FDA Regulations and State Regulations
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Standard Operating Procedure
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eLearning Development and Design
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Pod Casting Development and Design
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Negotiating for Clinical Researchers
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 Fraud and Misconduct in Clinical Research
# Clinical Research Process
# State & Federal Government regulations
# Budgeting and Contracting
# Financial Disclosure
# Safety Review and Reporting
# Adverse Event Recording and Reporting
# Developing a Clinical Monitoring Plan
# Site Non-compliance and Training
# Protocol Non-Compliance
# Fraud and Misconduct in Research
# Vendor Selection
# FDA and EMEA Audits

All courses have been developed at reasonable prices. Please call us at 610-341-9798 to discuss the details for your course.

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eLearning Modules

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Pharmaceutical development from Discovery to Marketing

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Clinical Research courses
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Good Clinical Practices

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Informed Consent

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EU CTD Overview
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ICH Guidelines Overview
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 Financial Disclosure
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 Computer Applications
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 Universal Precautions Training
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 Standard Operating Procedures

Pod Casts

Computer Application Training

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Oracle Clinical
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Clinical Trial Management Systems
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Clinical Supply Chain Systems
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Interactive Voice Randomization System

Specialty Programs and Courses

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“Six Sigma” project implementation training

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“On the Job” Training programs
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Mentoring Programs
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Interactive Voice Randomization System
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 “Just in Time” Help and eLearning systems
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 e-Simulations

Please call us at 610-341-9798 to discuss the details.
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