Grant-writing for Small Businesses

We offer a one-of-a-kind grantwriting service that is customizable to your specific needs. Furthermore, the current average return on investment for an accepted, SME-assisted grant is 1,205.04%.

Testimonials

What we provide: 

1

Administrative content and assistance with grant submission

2

Comprehensive grant review and editing with grant submission

3

Statistical analysis

4

Table and figure creation

5

Research bench-marking

6

Medical illustration

Based on previous applicants, the preparation and submission of a quality SBIR/STTR proposal takes more than 150 hours. As a support company, this must be a collaborative process. We’re looking for motivated partners who are willing to commit.
In order to work within our process,
You must:

Fill in the NIH-provided biosketch and budget templates

Write the aims page (we will edit it extensively)

Thoroughly review all material we generate and fill in as necessary

Provide all material in a timely manner and accord with internal deadlines

Submit the final manuscript

Our track record:

The return on investment for a risk-tolerant individual submitting a SBIR/STTR grants is extremely high

Superior Medical Experts has participated in the submission of twelve grants, several of which have been for the same client. Of the twelve submitted grants, four have been funded, with a total return of $1,417,000. Including failed submissions, the total cost to our clients of all grant-writing project was $58,559.

Disclaimer

Submitting a grant is an uncertain process, and the majority of grants are not accepted. Superior Medical Experts is looking to collaborate with risk-tolerant partners in all grant-writing enterprises, due to the unlikelihood of acceptance.

Our approach  provides comprehensive support while increasing grant submission productivity and eliminating overhead costs.

Our Process

 

1

A physician consultant who has served as a PI on SBIR/STTRs provides high-level feedback on the client’s aims page and research strategy.

 

2

Technically skilled medical writers with knowledge of clinical best practices help the client draft the research strategy from the aims page.

 

3

Once drafts of the scientific aspects are completed, a grant manager oversees the creation of compliance documents. These vary based on the FOA and study design; the client must supply all budgetary information.