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Meant for individuals in the United States, an IRB Certification can help to administer the regular activities of the Institutional Review Boards. For anyone who is a part of human subject research studies, it is mandatory to have a part of their identifiable data. Along with several other training modules, the process requires you to complete the CITI (Collaborative Institutional Training Initiative) Training. These training procedures must be renewed every few years.

What Are the Training Programs Required to Fulfil the IRB Training?

All the individuals who are a part of the research program with human participants must complete a series of training in order to get certified with the IRB Certification. Let’s have a look at a few training programs under the IRB Training.

Human Subjects Protection Training:

Before getting into the Review Research Office, one must complete the HSP training program. Upon successful completion of the same, a legal and certified copy of the same is retained by the authorities, and this is equivalent to proofreading.

A Good Clinical Practise Training:

Anyone who is engaged in the clinical trials of the research program is supposed to complete a good 3 years of GCP training. This training program is required in order to comply with the NIH Policy. Some of the vital components of the training program include the base clinical trial, the investigator and the clinical trial staff.

Learn Ecore is a commercially accredited review board. With expert compliance and ethical research training and programs, we offer a financial and non-financial topics of interest. Our sessions are available in English, French and Spanish.

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