![]() ![]() This cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Other. The cookies is used to store the user consent for the cookies in the category "Necessary". The cookie is set by GDPR cookie consent to record the user consent for the cookies in the category "Functional". The cookie is used to store the user consent for the cookies in the category "Analytics". The cookie is set by GDPR cookie consent to record the user consent for the cookies in the category "Advertisement". This cookie is set to enable shopping cart details on the site and to pass the data to our learning management system. This cookie is set to transfer purchase details to our learning management system. These cookies ensure basic functionalities and security features of the website, anonymously. Necessary cookies are absolutely essential for the website to function properly. ICH GUIDANCE SERIESOrganizational Subscription Price: Included in Good Clinical Practice (GCP) series for $1,000 per year/per site Independent Learner Price: $129 per person Demo Instructions ![]() ![]() Suggested Audiences: Clinical Research Coordinators, Contract Research Organizations (CROs), Investigators, IRB Members, Key Study Personnel, Oversight, Research Nurses, Research Staff who are Involved in the Design, Conduct, or Management of Clinical Trials with Drugs and/or Biologics, Sponsors Language Availability: Chinese, English, Korean, Spanish CITI Program offers several GCP courses that are considered acceptable by many leading organizations to meet their training needs per NIH policy released on 16 September 2016. The NIH does not endorse any specific training programs. * NIH in fulfillment of their GCP training policy (Policy on Good Clinical Practice Training for NIH Awardees Involved in NIH-funded Clinical Trials NOT-OD-16-148) states that NIH-funded investigators and staff should be trained in GCP. ICH GUIDANCE TRIALThe National Institutes of Health (NIH)* requires completion of GCP training that demonstrates that individuals have attained the fundamental knowledge of clinical trial quality standards for designing, conducting, recording, and reporting trials that involve human research participants. This course (English only) meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors.ĬITI Program GCP training is used by over 1,500 institutions – (including many leading hospitals, academic medical centers, universities, and healthcare companies) – to meet their GCP training needs. ICH GUIDANCE HOW TO
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