Opportunity Information: Apply for RFA EH 09 002
Apply for RFA EH 09 002
- The Centers for Disease Control and Prevention in the health sector is offering a public funding opportunity titled "Program to Expand State Public Health Laboratory Capacity for Newborn Bloodspot Screening (U01)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.064 Laboratory Training, Evaluation, and Quality Assurance Programs.
- This funding opportunity was created on Jan 21, 2009 and posted on Jan 21, 2009.
- Applicants must submit their applications by Mar 30, 2009 Letter of Intent Deadline February 19, 2009. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $1,000,000.00 to eligible and selected applicants.
- Each selected applicant is eligible to receive up to $500,000.00 in funding.
- The number of recipients for this funding is limited to 2 candidate(s).
- Eligible applicants include: City or township governments Native American tribal governments (Federally recognized) Native American tribal organizations (other than Federally recognized tribal governments) State governments Special district governments County governments.
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Opportunity Summary:
The CDC funding opportunity titled "Program to Expand State Public Health Laboratory Capacity for Newborn Bloodspot Screening (U01)" (Funding Opportunity Number RFA EH 09 002) is a discretionary cooperative agreement designed to help public health laboratories strengthen and modernize their newborn screening capabilities. The core aim is to support the development and refinement of new laboratory test methods that can be applied to newborn dried bloodspot screening, specifically targeting conditions that are not currently included on the American College of Medical Genetics (ACMG) recommended primary and secondary newborn screening panels. In practical terms, the program is about expanding what state and other governmental public health labs can reliably test for, improving the science and implementation readiness of emerging screening assays, and helping the public health system prepare for future additions to newborn screening programs.
The total estimated funding available for fiscal year 2009 is approximately $1,000,000, with CDC planning to make two awards. The implied budget structure sets an award ceiling of $500,000 per award, aligning with the plan for two recipients to split the overall allocation depending on final award decisions. Because the funding mechanism is a cooperative agreement (U01), recipients should expect substantial involvement from CDC compared with a typical grant. Cooperative agreements generally mean CDC will collaborate with awardees on technical direction, performance expectations, and coordination activities, which fits a program focused on developing and refining laboratory methods that may require standardized approaches, shared validation strategies, and strong quality practices.
Eligible applicants are limited to governmental and certain tribal entities, reflecting the public health laboratory focus of the program. Eligible organizations include state governments, county governments, city or township governments, special district governments, federally recognized tribal governments, and other tribal organizations. There is no cost-sharing or matching requirement, which reduces barriers for public sector laboratories that may not have flexible funds to meet match obligations. The program is listed under CFDA 93.064, which corresponds to CDC laboratory training, evaluation, and quality assurance programs, signaling that beyond pure research, the initiative is closely tied to laboratory quality systems, evaluation, and applied readiness for public health use.
Key dates indicate the opportunity was posted on January 21, 2009, with a letter of intent due February 19, 2009, and a full application closing date of March 30, 2009. The archive date is April 29, 2009, which typically means the opportunity was no longer active after that point for new submissions. CDC anticipated making awards before August 31, 2009, providing a clear timeline from submission to expected funding decisions. For applicants needing help accessing the announcement, CDC provided assistance through the Procurement and Grants Office Technical Information Management Section (PGOTIMS) at 770-488-2700.
Overall, this opportunity is best understood as an applied public health laboratory capacity-building and method-development effort centered on newborn bloodspot screening. It is intended to move potential new screening tests closer to real-world implementation by improving assay methods, performance, and suitability for state public health laboratory workflows, especially for conditions outside the then-current ACMG recommended panels.
Frequently Asked Questions (FAQs)
What is the name of this CDC funding opportunity?
The opportunity is titled "Program to Expand State Public Health Laboratory Capacity for Newborn Bloodspot Screening (U01)." The Funding Opportunity Number is RFA EH 09 002.
What type of funding mechanism is this?
This is a discretionary cooperative agreement (U01). A cooperative agreement typically involves substantial CDC involvement compared with a standard grant, including collaboration on technical direction, coordination, and performance expectations.
What is the main purpose of the program?
The core purpose is to help public health laboratories strengthen and modernize newborn screening capabilities by supporting the development and refinement of laboratory test methods that can be applied to newborn dried bloodspot screening.
What kinds of screening tests is this program focused on?
The focus is on developing and refining new laboratory test methods for conditions that are not currently included on the American College of Medical Genetics (ACMG) recommended primary and secondary newborn screening panels.
Is this opportunity about research, implementation, or both?
Based on the description, it is an applied public health laboratory capacity-building and method-development effort. It emphasizes improving assay methods, performance, and implementation readiness for public health laboratory workflows rather than research alone.
How does CDC expect to be involved with awardees?
Because this is a U01 cooperative agreement, CDC expects substantial involvement. The description suggests collaboration may include technical direction, performance expectations, coordination activities, and support for standardized approaches, shared validation strategies, and strong quality practices.
Who is eligible to apply?
Eligible applicants are limited to governmental and certain tribal entities. Eligible organizations include state governments, county governments, city or township governments, special district governments, federally recognized tribal governments, and other tribal organizations.
Are non-governmental organizations eligible to apply?
The eligibility list provided is limited to governmental and certain tribal entities. No other categories are identified in the provided information.
Is there a cost-sharing or matching requirement?
No. The opportunity states there is no cost-sharing or matching requirement.
How much funding is available?
The total estimated funding available for fiscal year 2009 is approximately $1,000,000.
How many awards does CDC plan to make?
CDC planned to make two awards.
What is the expected award size or ceiling?
The implied structure indicates an award ceiling of $500,000 per award, consistent with the plan to make two awards from an estimated total of $1,000,000.
What is the CFDA number for this program and what does it indicate?
The program is listed under CFDA 93.064. The description ties this to CDC laboratory training, evaluation, and quality assurance programs, indicating an emphasis on quality systems, evaluation, and applied readiness for public health laboratory use.
What is being screened and what specimen type is referenced?
The opportunity centers on newborn bloodspot screening, specifically mentioning newborn dried bloodspot screening as the application context for new or refined laboratory test methods.
What is the timeline for key submission dates?
The opportunity was posted on January 21, 2009. The letter of intent was due February 19, 2009. The full application closing date was March 30, 2009.
What does the archive date mean for this opportunity?
The archive date is April 29, 2009, which typically indicates the opportunity was no longer active for new submissions after that point.
When did CDC expect to make award decisions?
CDC anticipated making awards before August 31, 2009.
What kind of outcomes is this program trying to support?
The program is intended to move potential new screening tests closer to real-world implementation by improving assay methods, performance, and suitability for state public health laboratory workflows, and by helping the public health system prepare for future additions to newborn screening programs.
How does this opportunity relate to future newborn screening expansion?
It is framed as a way to help public health laboratories prepare for future additions to newborn screening programs by improving the science and implementation readiness of emerging screening assays, especially for conditions outside the then-current ACMG recommended panels.
Where can applicants get help accessing the announcement?
CDC provided assistance through the Procurement and Grants Office Technical Information Management Section (PGOTIMS) at 770-488-2700.
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