Opportunity Information: Apply for PA 13 052

  • The National Institutes of Health in the food and nutrition health sector is offering a public funding opportunity titled "Technological Improvements to Data Collection in NIDDK Kidney and Urology Clinical Studies (SBIR) (R43/R44)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.847 Diabetes, Digestive, and Kidney Diseases Extramural Research.
  • This funding opportunity was created on Feb 21, 2013 and posted on Dec 18, 2012.
  • Applicants must submit their applications by Jan 7, 2016. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Eligible applicants include: Small businesses.
Apply for PA 13 052

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Opportunity Summary:

The grant opportunity titled "Technological Improvements to Data Collection in NIDDK Kidney and Urology Clinical Studies (SBIR) (R43/R44)" (Funding Opportunity Number PA 13-052) is a National Institutes of Health (NIH) Small Business Innovation Research (SBIR) solicitation aimed at improving how clinical research data are captured in studies supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), specifically within kidney and urology clinical research. The central purpose is to fund small businesses to design, develop, and test practical tools that make clinical study data collection more efficient, more accurate, less burdensome for participants and study staff, and better suited for modern research workflows. In plain terms, NIH was looking for companies that could build devices, software, or enabling technologies that streamline the collection of source data used in NIDDK-funded clinical studies.

This opportunity uses the SBIR phased structure under the R43/R44 mechanisms, which generally aligns with early-stage feasibility work followed by more advanced development and validation. Phase I (R43) typically supports proof-of-concept and technical feasibility, while Phase II (R44) generally supports further development, refinement, and demonstration of performance in more realistic settings, such as pilot deployments in clinical study environments. The emphasis here is not on basic science, but on research and development that produces a tangible data-collection improvement that could be adopted by clinical researchers running kidney and urology studies. The technologies could involve better ways to capture clinical measurements, patient-reported outcomes, biospecimen-related metadata, workflow-integrated data entry, remote monitoring, or other approaches that reduce errors and missingness while improving timeliness and standardization.

Administratively, this is a discretionary grant opportunity offered by NIH, with the activity tied to the NIDDK extramural research portfolio (CFDA 93.847). It is explicitly limited to eligible small business applicants, and it does not require cost sharing or matching funds, which is typical for SBIR awards. The posting date was December 18, 2012, with a creation date of February 21, 2013. The original and final closing date listed is January 7, 2016, and the opportunity was archived on February 7, 2016, meaning it is no longer open for new applications under that particular announcement. For historical reference and full details, NIH provided the FOA text through its grants policy and guidance site at http://grants.nih.gov/grants/guide/pa-files/PA-13-052.html.

From an implementation standpoint, the kinds of projects that fit this FOA are those that directly address real pain points in clinical data acquisition for kidney and urology research: incomplete or inconsistent case report forms, burdensome manual transcription, poor integration with clinical systems, difficulties capturing longitudinal outcomes, and challenges collecting high-quality data outside the clinic. Strong applications typically would have proposed a clear technical approach, a plan to validate that the tool improves data quality or efficiency, and an adoption pathway showing how the product could be used in NIDDK-supported clinical studies. NIH also provided basic contact guidance through the NIH Office of Extramural Research (OER) webmaster for access or linking issues, indicating where applicants could get help if they had trouble reaching the full electronic announcement.

Frequently Asked Questions (FAQs)

What is the title and funding opportunity number for this grant?

The opportunity is titled "Technological Improvements to Data Collection in NIDDK Kidney and Urology Clinical Studies (SBIR) (R43/R44)" and the Funding Opportunity Number is PA 13-052.

Which agency is offering this opportunity?

This is a National Institutes of Health (NIH) funding opportunity.

Which NIH institute is associated with the program focus?

The opportunity is tied to the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), specifically within kidney and urology clinical research supported by NIDDK.

What is the main purpose of this SBIR solicitation?

The purpose is to fund small businesses to design, develop, and test practical tools that improve how clinical research data are captured in NIDDK-supported kidney and urology clinical studies. The goal is more efficient, more accurate, and less burdensome data collection for participants and study staff, aligned with modern research workflows.

What types of solutions was NIH looking for under this announcement?

NIH was looking for devices, software, or enabling technologies that streamline the collection of source data used in NIDDK-funded kidney and urology clinical studies.

Is this grant focused on basic science or product-oriented research and development?

The emphasis is not on basic science. It focuses on research and development intended to produce tangible improvements to clinical study data collection that could be adopted by clinical researchers conducting kidney and urology studies.

What funding mechanisms are used in this opportunity?

This opportunity uses the SBIR phased structure under the R43/R44 mechanisms.

What is the difference between Phase I (R43) and Phase II (R44) in this context?

Phase I (R43) typically supports proof-of-concept and technical feasibility. Phase II (R44) generally supports further development, refinement, and demonstration of performance in more realistic settings, such as pilot deployments in clinical study environments.

What areas of clinical data collection were highlighted as relevant?

Examples mentioned include better ways to capture clinical measurements, patient-reported outcomes, biospecimen-related metadata, workflow-integrated data entry, remote monitoring, and other approaches that reduce errors and missing data while improving timeliness and standardization.

What kinds of data-collection problems in kidney and urology studies was this intended to address?

The announcement emphasized real pain points in clinical data acquisition such as incomplete or inconsistent case report forms, burdensome manual transcription, poor integration with clinical systems, difficulties capturing longitudinal outcomes, and challenges collecting high-quality data outside the clinic.

Who is eligible to apply?

The opportunity is explicitly limited to eligible small business applicants (as an SBIR solicitation).

Is cost sharing or matching funding required?

No. The opportunity states that it does not require cost sharing or matching funds, which is typical for SBIR awards.

What is the CFDA number associated with this opportunity?

The CFDA number listed is 93.847.

What were the key dates for this funding opportunity?

The posting date was December 18, 2012. The creation date was February 21, 2013. The original and final closing date listed was January 7, 2016. The opportunity was archived on February 7, 2016.

Is this funding opportunity still open to new applications?

No. It was archived on February 7, 2016, and the final closing date listed is January 7, 2016, meaning it is no longer open under that particular announcement.

Where can someone find the full FOA text for reference?

The FOA text was provided by NIH at: http://grants.nih.gov/grants/guide/pa-files/PA-13-052.html

What characteristics were implied for a strong application?

Strong applications typically would have proposed a clear technical approach, included a plan to validate that the tool improves data quality or efficiency, and described an adoption pathway showing how the product could be used in NIDDK-supported clinical studies.

What kind of validation or testing was implied as important?

The description emphasizes designing, developing, and testing practical tools, with Phase II involving demonstration of performance in more realistic settings such as pilot deployments in clinical study environments.

Does the opportunity mention any support contact for access or linking problems?

Yes. NIH provided basic contact guidance through the NIH Office of Extramural Research (OER) webmaster for access or linking issues related to reaching the full electronic announcement.

What does it mean that this is a discretionary grant opportunity?

Based on the description provided, it is presented as a discretionary grant opportunity offered by NIH and tied to the NIDDK extramural research portfolio.

Browse more opportunities from the same agency: National Institutes of Health

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Next opportunity: RESEARCH OPPORTUNITIES IN AERONAUTICS 2013

Previous opportunity: Technological Improvements to Data Collection in NIDDK Kidney and Urology Clinical Studies (SBIR) (R41/R42)

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