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Investigator-Initiated Study (IIS) Grant Request Form

Supporting independent medical research that advances human health

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We proudly support researchers, clinicians and institutions that conduct research to advance medical treatment and the standard of care for patients. In an Investigator-Initiated Study, the investigator and/or institution assumes responsibility for all aspects of a study including patient safety and integrity of the data. IIS Grants are awarded based on scientific merit, including unmet medical need, as well as study feasibility and availability of funds. 

The following documentation is required during an IIS study proposal request:

  • Study protocol
  • Study budget
  • In the case of human subjects, IRB approval/exemption letter if obtained already

Prior to initiation of the IIS, the following will be required:

  • Fully executed investigator-initiated research agreement between the requesting organization and B. Braun
  • IRB approval/exemption letter if human subjects are involved

If your IIS falls within our areas of focus as described above, we invite you to request a Grant from B. Braun. For any questions, or if you encounter any problems, please send us an email at

Investigator-Initiated Study (IIS) Grant Request Form

Product shipping information (may not be to a personal address) if products are requested and if different from organization or principal investigator information provided above:

The following supporting documentation must be attached and submitted with the IIS Grant Request Form:


1. Study protocol *

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2. Study budget (if requesting money)

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3. IRS form W9 *

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4. If requesting products a complete list of the products requested using the product name (or SKU) and quantity of each. This information can be found on B. Braun’s website.

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By submitting this request, I acknowledge the B. Braun will require a signed agreement in the event my request is approved and before providing the approved support.


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