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This policy outlines the secure storage procedures for research records at the Portland VA Medical Center, detailing responsibilities for record maintenance and interaction with the National Archives.
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How to fill out research records storage policy

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How to fill out Research Records Storage Policy

01
Begin by gathering all necessary information regarding the research project.
02
Clearly define the types of records that will be stored, such as data sets, consent forms, and analysis results.
03
Specify the retention period for each type of record, following regulatory and institutional guidelines.
04
Identify the secure storage methods that will be used for physical and electronic records.
05
Outline access controls to ensure that only authorized personnel can access the records.
06
Include protocols for regular review and disposal of records that are no longer needed.
07
Ensure compliance with any relevant legal, ethical, or institutional policies.
08
Document the policy clearly, using straightforward language for all stakeholders.

Who needs Research Records Storage Policy?

01
Researchers managing data from studies or experiments.
02
Institutional review boards overseeing ethical research practices.
03
Compliance officers ensuring adherence to regulations.
04
Administrative staff responsible for record-keeping and storage.
05
Research collaborators who need to access shared data.
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A period of at least 2 years following the date on which an application for a research or marketing permit, in support of which the results of the nonclinical laboratory study were submitted, is approved by the Food and Drug Administration.
Minimum three years for all types of studies.
The HIPAA retention requirements are that certain types of documents must be maintained for six years from the date of their creation or from the date on which they were last in effect, whichever is later.
Under the GDPR, there is no specific retention period prescribed; instead, data must be kept no longer than necessary to fulfil the purposes for which it was collected. The retention period depends on various factors, including legal obligations, the purpose of data processing, industry standards, and business needs.
The length of time you store data depends on the nature of the research project and the resultant data. Where it is workable, you should store all data (for at least the term of the project). Most researchers will store data for at least five years after final publication.
Those recipients must retain the records pertinent to the entire competitive segment for 3 years from the date the FFR is submitted to NIH.
Research records should be retained, generally, for a period of no fewer than seven (7) years after the end of a research project or activity; for specific guidance on how long to retain different types of records or to obtain assistance with handling records that have met their mandated retention periods, contact

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The Research Records Storage Policy outlines the guidelines and procedures for the proper storage, management, and retention of research records to ensure compliance with legal, ethical, and institutional requirements.
All researchers, faculty, and staff involved in conducting research that generates records must file the Research Records Storage Policy to ensure adherence to institutional standards.
To fill out the Research Records Storage Policy, individuals must provide relevant details about the research project, specify the types of records being maintained, outline storage methods, and indicate retention periods.
The purpose of the Research Records Storage Policy is to protect research integrity, ensure data security, facilitate access to records, and comply with regulatory and funding agency requirements.
The information that must be reported includes the title of the research project, principal investigator's name, types of research records, storage location, retention timeline, and any pertinent legal or ethical considerations.
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