Ready to begin your project? All listed forms and rules are up to date for the 2024-2025 season!
ISEF 2024-2025 Rules All 2024-2025 Forms Packet ISEF Rules Wizard Do I need pre-approval? AI Use Policy
Curious about what is new in this year's ISEF Forms and Rules? Read more here!
Forms Required for All Projects
TIP: The checklist is provided so that the adult sponsor can review what information (and therefore which forms) must be provided. The date signed is the date that the sponsor first reviews the project plan before the experiment begins.
TIP: On this page, the student outlines what the project is about. Items that especially need to be clear are the following:
#5 Any project conducted in a similar area of research as previous projects should be considered a continuation. If the project is a continuation, explain on Form 7 as completely as possible how the project will differ from previous experimentation because ONLY a new and different research project is allowed. The current year project must demonstrate significant progress.
#6 Explain when the actual experimental procedure (not the background literature review) will begin and end because ONLY a 12-month project that occurred within the last 18 months before this Intel ISEF is allowed.
#7 Explain where the experimental research will be done: research institution, school, field, home. Universities, research facilities, and industrial settings will require additional documentation on Form 1C to explain what was done at each facility. (Note: Pathogens may NOT be cultured at home.)
#9 Attach a research plan, as outlined in the Research Plan Instructions, which describes the project in detail and answers all applicable questions.
TIP: These statements attest that each of these people (or committees) approves or consents to this project. The dates should be signed as described below and are before experimentation unless otherwise indicated:
Student | Date they attest that they understand the possible risks, that they have read and will follow the rules, and that they will abide by the ethics statement. |
Parent/Guardian | Date they consent to their child doing this project. |
SRC Approval BEFORE | Date that the committee reviews this project BEFORE the experimentation. Projects that must be preapproved are research in these areas: human subjects, vertebrate animals, and PHBA’s (potentially hazardous pathogenic agents) including microorganisms, recombinant DNA, and human or animal tissue. |
SRC Approval AFTER | This applies only to projects that needed preapproval by the SRC but were done at a research institution and were preapproved by that institution instead of the affiliated fair SRC. The date signed indicates when the SRC approved this project after it was completed. All documentation from the research institution showing approval of the project must be attached. |
Final SRC Approval | All projects must be reviewed by the SRC after the experimentation is complete and shortly BEFORE competition in the affiliated fair. The date signed shows the date that SRC gives final approval to this project. |
TIP: Required for projects using hazardous chemicals, activities or devices, and some PHBA’s including protists, composting, coliform test kits, and decomposition of vertebrate organisms and must be completed and signed by the DS or QS prior to student experimentation.
Project-Dependent Forms
TIP: This form is completed by the supervising adult, explains what the student researcher actually did and is signed after the project is completed. This form is only needed if the research was done at a research institution (university lab, for example) or in an industrial setting, but is not completed for work done at a high school.
TIP: On this page, the scientist explains what will be done to oversee this project. The qualified scientist (QS) and, if needed, the designated supervisor (DS), will sign with the date that they approve this project (before experimentation takes place).
TIP: This page, along with the research plan, is submitted by the student researcher to explain to the IRB how the safety and well being of the test subjects and the confidentiality of results will be ensured. The IRB reviews the project, checks the risk level and determines if written participant consent/permission was properly documented. Please understand ALL human participants must have given writen concent to participate in any data collection! All questions must be answered and boxes checked. Each IRB member signs with the date they approve this project. This review and the date signed must be BEFORE any experimentation takes place.
TIP: This page, Form 4, along with the research plan, is submitted by the student researcher to explain to the IRB how the safety and well being of the test subjects and the confidentiality of results will be ensured. The IRB reviews the project, checks the risk level and determines if written documentation of consent/permission is required. All questions must be answered and boxes checked above the "Voluntary Participation" section.
See how Jane Smith filled out the Human Informed Consent form
TIP: This form is filled out by the student researcher when the experiment is conducted in a Non-Regulated Research Site such as home or school and describes the housing and care for the animals. The SRC reviews this document and determines the level of supervision required for the study and signs and dates BEFORE experimentation begins. The bottom of the form is filled out by the veterinarian and/or designated supervisor and is signed and dated when they approve this project with these housing conditions. (Before experimentation begins.) If there was any weight loss or death of an animal during the experimentation, the cause must be investigated and a letter from the Qualified Scientist, Designated Supervisor, or a veterinarian which documents the situation and the results of the investigation must be attached.
TIP: This form is filled out by the student researcher when the experiment is conducted in a Regulated Research Site (Anywhre other than home, feild, or school). The SRC reviews this document and determines the level of supervision required for the study and signs and dates BEFORE experimentation begins. The bottom of the form is filled out by the veterinarian and/or designated supervisor and is signed and dated when they approve this project with these housing conditions. (Before experimentation begins.) If there was any weight loss or death of an animal during the experimentation, the cause must be investigated and a letter from the Qualified Scientist, Designated Supervisor, or a veterinarian which documents the situation and the results of the investigation must be attached.
This form is filled out by the student researcher and is required for all research involving microorganisms, rDNA and fresh/frozen tissue (including primary cell lines, human and other primate established cell lines and tissue cultures), blood, blood products, and body fluids. SRC/IACUC/IBC/RAC approval required BEFORE experimentation. The qualified scientist will sign and date. The SRC will choose one or more statements that describe the approval process for the study and will add the date that approval occurred.
This form is filled out by the student researcher and explains the source of the tissue. The Qualified Scientist or Designated Supervisor signs and dates to document the source and handling of this tissue (before experimentation).
TIP: If the current project is in a similar area of research as any previous project of the student or any team member, it is considered a continuation. Explain as completely as possible how the project is different from previous experimentation because ONLY a new and different research project is allowed. The date signed is the date the student researcher is certifying that this information is correct.
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