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IRB Approved: 10/17/2012 Expiration Date: 05/01/2013 COR IHS, Stony Brook University Committees on Research Involving Human Subjects Established 1971 Title of Study: Non Transplant Tissue Bank Principal
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Start by gathering all the necessary information and documents. You will need to have the IRB approved 10172012 expiration form, any relevant supporting documents, and any other required paperwork.
02
Begin by carefully reading the instructions provided on the form. Make sure you understand what information is being asked for and the specific format in which it should be provided.
03
Fill in your personal information, such as your name, contact details, and any other required identification information. Ensure that the information you provide is accurate and up-to-date.
04
Provide the necessary details about the research project or study that is associated with the IRB approval. This may include the project title, the principal investigator's name, the purpose of the study, and any other relevant information.
05
Indicate the date of the IRB approval. In this case, it should be 10172012, as specified in the form title.
06
Provide any additional required information or documentation that is necessary for the expiration process. This may include any updates or changes to the research study since the initial approval, any adverse events or incidents that occurred during the study, or any other required reporting.
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Review your completed form to ensure that all the required fields have been filled out accurately and completely. Double-check for any mistakes or missing information.
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Who needs IRB approved 10172012 expiration?

The IRB approved 10172012 expiration is typically needed by individuals or organizations who conduct research studies involving human subjects. This may include researchers from academic institutions, hospitals, pharmaceutical companies, or any other entity that engages in human subjects research.
The expiration date refers to the date at which the IRB approval granted for a research study expires. It is important to renew this approval before the expiration date to ensure that the study can continue to be conducted in compliance with ethical guidelines and regulations.
Failure to renew the IRB approval before the expiration date may result in the suspension or termination of the research study. It is the responsibility of the study's principal investigator and research team to ensure that the expiration date is monitored and that the necessary steps are taken to renew the approval when needed.
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IRB approved 1017 expiration refers to the expiration date of the Institutional Review Board approval for a research study.
The principal investigator of the research study is responsible for filing the IRB approved 1017 expiration.
The IRB approved 1017 expiration form typically requires information regarding the study protocol, any modifications made, and the current status of the research.
The purpose of the IRB approved 1017 expiration is to ensure that research studies are being conducted ethically and in accordance with regulations and guidelines.
The IRB approved 1017 expiration form may require information such as the study title, principal investigator, study status, and any adverse events that have occurred.
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