Get Electronic Version Of The Form Nih-2803-1 With Instructions - Home Ccr Cancer 2020-2025

Filling out the Electronic Version Of The Form NIH-2803-1 is essential for the procurement of human biological materials for research. This guide provides clear, step-by-step instructions on completing each section of the form to ensure accurate submissions.

Follow the steps to successfully complete the NIH-2803-1 form online.

1. Click ‘Get Form’ button to obtain the form and open it in the editor.
2. Complete one form for each procurement procedure. Be sure to provide patient identification information, including last name, first name, middle initial, and NIH medical record number in the designated area at the bottom left corner of the form.
3. Print the IRB Protocol Number associated with the research specimen collection, along with the designated principal investigator’s (PI) first and last name. Remember, a separate form is required for each IRB protocol number.
4. Add the designated PI’s telephone number and pager number to ensure they can be contacted immediately if necessary.
5. Indicate the date on which the specimen will be collected.
6. Select only one checkbox to specify whether the specimen(s) collected will be for 'Research Use Only' or for 'Research and Diagnostic/Transplant Purposes' such as a split sample.
7. Provide a description of the anticipated research sample(s).
8. Indicate the name and contact numbers of the person designated to pick up the sample.
9. Specify the storage site for the specimen(s), including laboratory name, location, and contact number.
10. Include any special instructions regarding the specimen(s), such as storage conditions or handling procedures.
11. Ensure the principal investigator or an associate investigator signs the request, certifying that the specified IRB approval encompasses both the protocol and consent documents. Be sure to print the name and date this signature.
12. Before the specimens are collected, insert the signed form into the patient's medical record jacket before their arrival for the procedure.
13. After procurement, document the release date of the specimen at the lower portion of the form and detail each specimen collected in the respective order.
14. Send the signed form to the appropriate designations as noted in the instructions, ensuring a copy goes with clinical specimens when necessary.
15. Finally, save your changes, download, print, or share the completed form as required.

Complete your documents online now for efficient management and compliance.