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The form templates are available here so that the requestor may become familiar with the information which will be requested on web request forms. The templates are not editable and cannot be used to submit a request. You may submit a request from our list of Currently Available Collections.

Request Biospecimens and Data (Readonly)

If you are interested in requesting specific collection biospecimens and data from NIA, update and submit the form below and a member of the AgingResearchBiobank staff will contact you within 7-10 days. If desired, you may save the form instead and return to complete it at a later time. For further details regarding the request workflow, please refer to the User's Guide (PDF - 1,678 KB).

If you do not have funding and require a letter of availability for a grant proposal, please note this in the "Support Information" section below. Note that the repository generally prepares reports within six weeks of receiving criteria applicable to the requested studies.

Once you have funding available please contact us through the Comments section of your request to continue with your request.

If you already have funding, you will need to complete the required fields below and provide the following documentation before your request is reviewed by the Biobank Scientific Review Committee (BSRC):

  1. Protocol (See Glossary for more information)
  2. IRB Approval (or waiver)
  3. CV
  4. Proof of Funding

The BSRC will review requests three times a year in the months of January, May, and September. The BSRC will only review a request that has submitted all of the required documentation, noted above. The documents submitted will be examined to ensure they comply with NIA requirements prior to the BSRC's review. If documents are missing your submitted request will not be reviewed by the BSRC until the documentation is complete or until the next BSRC meeting period. The online application as well as all required documentation must be submitted prior to the following dates to be included in the BSRC review period:

  1. BSRC Review Period 1 (2024) Deadline: January 15th, 2024
  2. BSRC Review Period 2 (2024) Deadline: May 15th, 2024
  3. BSRC Review Period 3 (2024) Deadline: September 15th, 2024

If your request is approved, the Outgoing Human Resources Transfer Agreement (OHRTA) will need to be signed by the PI and the institution's signing official.

All fields are required.

Request Identifier
Full title for the proposed research
Requestor Information

Brief summary (1-2 sentences) of the proposed research to be made public if the request is approved. A more detailed summary and protocol are also required separately in the Request Details section below. (Limit 500 characters)

Principal Investigator Information
The Principal Investigator (PI) must have the level of authority and oversight responsibility to fulfill the OHRTA/OHDTA requirements for that role. Students and temporary staff are not eligible to sign the OHRTA/OHDTA as the PI. Please designate a faculty advisor or supervisor as the study PI, and include the names and titles of the student or temporary staff among the Other Authorized Users.
Authorized Users
Signing Official Information
A Signing Official (SO) from your institution will be asked to provide their signature in the transfer agreement. An SO has institutional authority to legally bind the institution in grants administration matters. The individual fulfilling this role may have any number of titles in the grantee organization. For most institutions, the SO is located in its Office of Sponsored Research or equivalent.
Specimen Shipping Information
*Note: Specimens will be shipped to the above address. Specimens cannot be shipped to a post office box.
Support Information
Is funding currently available for this research?
Do you require a letter of biospecimen availability for inclusion in a grant application?
Please specify if you require a letter by a certain date. Note that a letter is generally prepared within six weeks of receiving criteria applicable to the requested study.
Institution Type
Number of years in scientific research
Approximately how many years has the lead investigator been involved in scientific research?
If funding is not yet available, please indicate anticipated primary funding source.
If funding is non-NIH, please attach supporting documentation below.
Request Details
Please select the studies you would like to request. If requesting SWAN, that is the only study you may request.
Have you previously acquired data, images, or biospecimens from the study collection(s) being requested?
Does your proposal require linking biobank materials to the existing data, images, or biospecimens described above?
A brief overview of your research needs. This is in addition to the full protocol to be attached below.
Describe any additional requirements pertaining to the biospecimens themselves, such as anticoagulant used, additives, preservatives, etc.
Describe the characteristics of the subjects to be searched for available specimens. Criteria might include gender, age, disease status, genotype, etc. Be as specific as possible.
Only applicable for studies that have more than one specimen draw point. If any visit is acceptable, please indicate so. Refer to the "Available Biospecimens" tables on each study description page for more information regarding the available visits for each material type. If more than one visit is requested, please indicate if you can accept subjects that have specimens available from at least one, but not all of the requested visits.
Approximate count of subjects required for your study. This may be the same as the number of specimens if only one draw and material type is needed per subject.
Approximate count of specimens required for your study. This may be more than the number of subjects if more than one draw and/or material type is needed per subject.
Please include units.
Please include units.
Describe the assay(s) to be performed and include any test volume requirements.
Describe the assay kit(s)/platform(s) to be used, if applicable.
Also describe your intended use of covariates from study datasets, if applicable.
Will the results be used for a commercial purpose?
A "Yes" response defines this as a "Commercial Purpose" request.
Original Study Investigator?
Were you an investigator with the original (parent) study(ies) referenced in this request?
Information Security: Please check the information security practices to be used
Study data must be maintained in a secure and controlled environment
Will anyone else besides the PI and authorized users noted above have access to these data or specimens, including lab personnel?
e.g. Amazon Web Services, Microsoft Azure, Google Cloud Platform / what tools will be used and how these tools relate to the project