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• Certification Preparation Packages
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• On-Line Clinical Research Associate Training (CRA)
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• On-Line Project Management Training
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000 Shipping within the Continental US
5-7 day shipping to addresses within the continental US is free. For OVERNIGHT SHIPPING or shipping to all other locations, please add your shipping choice from the Shipping and Handling Link on the left.
Price:  $0.00
801 Certification Preparation Pack for Monitors

 
Bundle includes:
Item 501 Step-by-Step Guide to Clinical Trials for Sponsors and Monitors150 page guide describing over 70 steps required to support the GCP-compliant conduction of clinical trials for sponsors and monitors, based on US and ICH requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Price:  $375.00
801-T Certification Preparation Pack for Monitors with On line Practice Test

 
Bundle includes:
Item 501 Step-by-Step Guide to Clinical Trials for Sponsors and Monitors150 page guide describing over 70 steps required to support the GCP-compliant conduction of clinical trials for sponsors and monitors, based on US and ICH requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Item RAN 5102T GCP Practice Test100 question practice test with feedback on general GCP requirements, adverse events, informed consent, institutional review boards, investigational supplies, protocol implementation, monitoring and study documentation from both ICH and FDA perspectives.
Price:  $450.00
803 Certification Preparation Pack for Investigators & Coordinators

 
Bundle includes:
Item 502 Step-by-Step Guide to Clinical Trials for Investigators and Coordinators150 page guide describing over 70 steps required to support the GCP-compliant conduction of clinical trials for investigators and clinical research coordinators based on US and ICH requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Price:  $375.00
803-T Certification Preparation Pack for Investigators & Coordinators with On-line Practice Test

 
Bundle includes:
Item 502 Step-by-Step Guide to Clinical Trials for Investigators and Coordinators150 page guide describing over 70 steps required to support the GCP-compliant conduction of clinical trials for investigators and clinical research coordinators based on US and ICH requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Item RAN 5102T GCP Practice Test100 question practice test with feedback on general GCP requirements, adverse events, informed consent, institutional review boards, investigational supplies, protocol implementation, monitoring and study documentation from both ICH and FDA perspectives.
Price:  $450.00
806 The Ultimate Certification Preparation Package for Coordinators
Continuing education contact hours are provided by The RAN Institute, Inc. Provider approved by the California Board of Registered Nursing, Provider #14637, for 8 Contact Hours. The course test 8002T must be succesfully completed to receive contact hours.
 
Bundle includes:
ASKA-RAN 8002 GCP Training for the Clinical Research Coordinator with Nursing Contact HoursComprehensive GCP training for clinical research coordinators.
ASKA-RAN 8002T GCP Training for the Clinical Research Coordinator with CE TESTCourse test for RAN 8002T. A certificate of completion is available for students achieving a passing score.
Item 502 Step-by-Step Guide to Clinical Trials for Investigators and Coordinators150 page guide describing over 70 steps required to support the GCP-compliant conduction of clinical trials for investigators and clinical research coordinators based on US and ICH requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Item RAN 5102T GCP Practice Test100 question practice test with feedback on general GCP requirements, adverse events, informed consent, institutional review boards, investigational supplies, protocol implementation, monitoring and study documentation from both ICH and FDA perspectives.
Price:  $650.00
808 The Ultimate Certification Preparation Package for Coordinators for Canada
Continuing education contact hours are provided by The RAN Institute, Inc. Provider approved by the California Board of Registered Nursing, Provider #14637, for 8 Contact Hours. The course test 8002T must be succesfully completed to receive contact hours.
 
Bundle includes:
ASKA-RAN 8002 GCP Training for the Clinical Research Coordinator with Nursing Contact HoursComprehensive GCP training for clinical research coordinators.
ASKA-RAN 8002T GCP Training for the Clinical Research Coordinator with CE TESTCourse test for RAN 8002T. A certificate of completion is available for students achieving a passing score.
Item 505 Canadian Edition of Step-by-Step Guide to Clinical Trials for Investigators and CoordinatorOver 150 page guide describing more than 70 steps required to support the GCP-compliant conduction of clinical trials for investigators and clinical research coordinators in Canada. Also includes US and ICH GCP requirements.
Item 700 All GCP Flash Card PackageOver 950 flash cards covering 21 CFR 11, 21 CFR 50, 21 CFR 54, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Guideline for the Monitoring of Clinical Investigations, and the ICH GCP Guideline E6. Save over 10% with this package.
Item RAN 5102T GCP Practice Test100 question practice test with feedback on general GCP requirements, adverse events, informed consent, institutional review boards, investigational supplies, protocol implementation, monitoring and study documentation from both ICH and FDA perspectives.
Price:  $650.00