The Center for Drug Evaluation and Research (CDER) is offering grants to develop non-proprietary, consensus-based data standards for human drug development and evaluation, aiming to improve the efficiency and effectiveness of regulatory processes. Projects will focus on clinical and nonclinical study data standards, therapeutic areas, and regulatory submission sections. Applicants must submit a detailed program plan, method for tracking progress, scope of work, collaboration strategies, alignment with existing standards, and PI experience. Priority is given to projects addressing therapeutic areas with high drug development activity. The deadline for applications is June 16, 2014. For more information, visit the provided link.
Opportunity ID: 254499
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | RFA-FD-14-004 |
| Funding Opportunity Title: | Data Concepts and Terminology Standards for Clinical Research and Drug Development (U24) |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health Information and Statistics Science and Technology and other Research and Development |
| Category Explanation: | – |
| Expected Number of Awards: | 4 |
| Assistance Listings: | 93.103 — Food and Drug Administration_Research |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 2 |
| Posted Date: | Apr 29, 2014 |
| Last Updated Date: | May 16, 2014 |
| Original Closing Date for Applications: | Jun 16, 2014 |
| Current Closing Date for Applications: | Jun 16, 2014 |
| Archive Date: | Jul 16, 2014 |
| Estimated Total Program Funding: | $1,000,000 |
| Award Ceiling: | $225,000 |
| Award Floor: | $200,000 |
Eligibility
| Eligible Applicants: | Small businesses Others (see text field entitled “Additional Information on Eligibility” for clarification) For profit organizations other than small businesses Public and State controlled institutions of higher education State governments Native American tribal organizations (other than Federally recognized tribal governments) Public housing authorities/Indian housing authorities City or township governments Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Private institutions of higher education County governments Independent school districts Special district governments Native American tribal governments (Federally recognized) |
| Additional Information on Eligibility: | Foreign Organizations |
Additional Information
| Agency Name: | Food and Drug Administration |
| Description: | The Center for Drug Evaluation and Research (CDER) receives a vast and growing amount of data in a variety of regulatory submissions from a multitude of sources and in a variety of formats. This wealth of data holds great potential to advance CDERs regulatory and scientific work, but the present lack of standardized data creates significant challenges to realizing that potential. The volume and complexity of drug-related information submitted to CDER for regulatory review is creating significant challenges to the Centers ability to efficiently and effectively perform its critical public health mission.The lack of standardized data affects CDERs review processes by curtailing a reviewers ability to perform integral tasks such as rapid acquisition, analysis, storage and reporting of regulatory data. Improved data quality, accessibility and predictability will give reviewers more time to carry out complex analyses, ask in-depth questions and address late-emerging issues. Standardized data will allow reviewers to increase review consistency and perform evaluations across the drug lifecycle. This will enhance the Centers performance across key drug regulatory functions and ongoing business operations, including pre-market review, post-market safety, oversight of drug quality, and oversight of drug promotion.In accordance with the Office of Management and Budget (OMB) Circular A-119, the FDA will: use voluntary, consensus-based standards development processes in place of government unique standards unless such standards are inconsistent with law or otherwise impractical; advocate to align these standards with existing health information technology initiatives, laws, regulations, and mandates; and promote coordination with other standards currently in use. The projects selected under this funding opportunity must adhere to these principles.OVERARCHING PROGRAM GOAL:The CDER Data Standards Program’s goals are: Support open, consensus-based data standards development Maintain and promote a well-defined data standards governance function Promote the electronic submission of regulatory data using established standards Optimize the regulatory review process to fully leverage data conformed to standards PROGRAM PRIORITIES:The Food and Drug Administration is announcing the availability of cooperative agreements for the development of data concepts and terminology standards to support human drug development and evaluation. The primary objective is to support the development of non-proprietary, consensus-based data standards for use in clinical studies of human drugs and biologics. Projects may focus on the identification of solutions to data standards development and their challenges in areas, such as general clinical and nonclinical study data, specific therapeutic areas, as well as other sections of the regulatory submission (e.g., quality / Chemistry, Manufacturing, and Controls (CMC)).DESCRIPTION:The application must include:An overall program plan describing the approach, process to be used in developing the selected area for standardization, any specific technologies to be utilized and experience with those technologies, and deliverables A method (e.g., Gantt chart) to plan and track progress toward specific deliverables under this award for the purpose of reporting the status to the FDA and its stakeholders. At a minimum, information reported should include a listing of interim steps necessary to complete a given deliverable, the timeline for completing those tasks, and a report of any issues in meeting those established deadlines. Definition of scope to be addressed (e.g., use case) during the project period Description of the result (concept, terminology, domain, therapeutic area) to be developed in the application (e.g., completed implementation guide) Description of the coordination/collaboration (to achieve consensus) needed to address the area of standardization including by not limited to: engagement of subject matter experts, organizations, standards development organizations, affected stakeholdersHow the standard being addressed aligns with currently available standards and approach to making the standard publically available A description of the experience of the principal investigators (PI), who is/are the Program Director (PD), should be described, together with his/her/their involvement in the projects. It is expected that PI(s) should have experience with data standards development as the PI(s) have the ultimate responsibility for the successful outcomes of the projects Specific Areas of Research Interest: FDA/CDER is specifically interested in projects to develop standardized clinical research concepts and terminology for therapeutic areas with significant drug development pipeline activity, emerging or complex analytical challenges, and/or are of significant public health concern. The list of therapeutic areas with current status is available at: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/ucm287408.htm. |
| Link to Additional Information: | Copy of published RFA |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Gladys Melendez-Bohler
Grants Management Officer/Specialist Phone 240-402-7565 Email:gladys.bohler@fda.hhs.gov |
Version History
| Version | Modification Description | Updated Date |
|---|---|---|
| The Project Officer’s correct e-mail is: Jenise Gillespie-Pedersen@fda.hhs.gov
She can be reached at 301-796-4211. The Grants Management Specialist, Gladys.bohler@fda.hhs.gov can be reached at 240-402-7565 (new number) |
May 16, 2014 | |
| May 16, 2014 |
DISPLAYING: Synopsis 2
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | RFA-FD-14-004 |
| Funding Opportunity Title: | Data Concepts and Terminology Standards for Clinical Research and Drug Development (U24) |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health Information and Statistics Science and Technology and other Research and Development |
| Category Explanation: | – |
| Expected Number of Awards: | 4 |
| Assistance Listings: | 93.103 — Food and Drug Administration_Research |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 2 |
| Posted Date: | Apr 29, 2014 |
| Last Updated Date: | May 16, 2014 |
| Original Closing Date for Applications: | Jun 16, 2014 |
| Current Closing Date for Applications: | Jun 16, 2014 |
| Archive Date: | Jul 16, 2014 |
| Estimated Total Program Funding: | $1,000,000 |
| Award Ceiling: | $225,000 |
| Award Floor: | $200,000 |
Eligibility
| Eligible Applicants: | Small businesses Others (see text field entitled “Additional Information on Eligibility” for clarification) For profit organizations other than small businesses Public and State controlled institutions of higher education State governments Native American tribal organizations (other than Federally recognized tribal governments) Public housing authorities/Indian housing authorities City or township governments Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Private institutions of higher education County governments Independent school districts Special district governments Native American tribal governments (Federally recognized) |
| Additional Information on Eligibility: | Foreign Organizations |
Additional Information
| Agency Name: | Food and Drug Administration |
| Description: | The Center for Drug Evaluation and Research (CDER) receives a vast and growing amount of data in a variety of regulatory submissions from a multitude of sources and in a variety of formats. This wealth of data holds great potential to advance CDERs regulatory and scientific work, but the present lack of standardized data creates significant challenges to realizing that potential. The volume and complexity of drug-related information submitted to CDER for regulatory review is creating significant challenges to the Centers ability to efficiently and effectively perform its critical public health mission.The lack of standardized data affects CDERs review processes by curtailing a reviewers ability to perform integral tasks such as rapid acquisition, analysis, storage and reporting of regulatory data. Improved data quality, accessibility and predictability will give reviewers more time to carry out complex analyses, ask in-depth questions and address late-emerging issues. Standardized data will allow reviewers to increase review consistency and perform evaluations across the drug lifecycle. This will enhance the Centers performance across key drug regulatory functions and ongoing business operations, including pre-market review, post-market safety, oversight of drug quality, and oversight of drug promotion.In accordance with the Office of Management and Budget (OMB) Circular A-119, the FDA will: use voluntary, consensus-based standards development processes in place of government unique standards unless such standards are inconsistent with law or otherwise impractical; advocate to align these standards with existing health information technology initiatives, laws, regulations, and mandates; and promote coordination with other standards currently in use. The projects selected under this funding opportunity must adhere to these principles.OVERARCHING PROGRAM GOAL:The CDER Data Standards Program’s goals are: Support open, consensus-based data standards development Maintain and promote a well-defined data standards governance function Promote the electronic submission of regulatory data using established standards Optimize the regulatory review process to fully leverage data conformed to standards PROGRAM PRIORITIES:The Food and Drug Administration is announcing the availability of cooperative agreements for the development of data concepts and terminology standards to support human drug development and evaluation. The primary objective is to support the development of non-proprietary, consensus-based data standards for use in clinical studies of human drugs and biologics. Projects may focus on the identification of solutions to data standards development and their challenges in areas, such as general clinical and nonclinical study data, specific therapeutic areas, as well as other sections of the regulatory submission (e.g., quality / Chemistry, Manufacturing, and Controls (CMC)).DESCRIPTION:The application must include:An overall program plan describing the approach, process to be used in developing the selected area for standardization, any specific technologies to be utilized and experience with those technologies, and deliverables A method (e.g., Gantt chart) to plan and track progress toward specific deliverables under this award for the purpose of reporting the status to the FDA and its stakeholders. At a minimum, information reported should include a listing of interim steps necessary to complete a given deliverable, the timeline for completing those tasks, and a report of any issues in meeting those established deadlines. Definition of scope to be addressed (e.g., use case) during the project period Description of the result (concept, terminology, domain, therapeutic area) to be developed in the application (e.g., completed implementation guide) Description of the coordination/collaboration (to achieve consensus) needed to address the area of standardization including by not limited to: engagement of subject matter experts, organizations, standards development organizations, affected stakeholdersHow the standard being addressed aligns with currently available standards and approach to making the standard publically available A description of the experience of the principal investigators (PI), who is/are the Program Director (PD), should be described, together with his/her/their involvement in the projects. It is expected that PI(s) should have experience with data standards development as the PI(s) have the ultimate responsibility for the successful outcomes of the projects Specific Areas of Research Interest: FDA/CDER is specifically interested in projects to develop standardized clinical research concepts and terminology for therapeutic areas with significant drug development pipeline activity, emerging or complex analytical challenges, and/or are of significant public health concern. The list of therapeutic areas with current status is available at: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/ucm287408.htm. |
| Link to Additional Information: | Copy of published RFA |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Gladys Melendez-Bohler
Grants Management Officer/Specialist Phone 240-402-7565 Email:gladys.bohler@fda.hhs.gov |
DISPLAYING: Synopsis 1
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | RFA-FD-14-004 |
| Funding Opportunity Title: | Data Concepts and Terminology Standards for Clinical Research and Drug Development (U24) |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health Information and Statistics Science and Technology and other Research and Development |
| Category Explanation: | – |
| Expected Number of Awards: | 4 |
| Assistance Listings: | 93.103 — Food and Drug Administration_Research |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 1 |
| Posted Date: | May 16, 2014 |
| Last Updated Date: | – |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | Jun 16, 2014 |
| Archive Date: | Jul 16, 2014 |
| Estimated Total Program Funding: | $1,000,000 |
| Award Ceiling: | $225,000 |
| Award Floor: | $200,000 |
Eligibility
| Eligible Applicants: | Others (see text field entitled “Additional Information on Eligibility” for clarification) City or township governments Public and State controlled institutions of higher education Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Independent school districts State governments Special district governments Native American tribal governments (Federally recognized) Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Small businesses For profit organizations other than small businesses County governments Private institutions of higher education Public housing authorities/Indian housing authorities Native American tribal organizations (other than Federally recognized tribal governments) |
| Additional Information on Eligibility: | Foreign Organizations |
Additional Information
| Agency Name: | Food and Drug Administration |
| Description: | The Center for Drug Evaluation and Research (CDER) receives a vast and growing amount of data in a variety of regulatory submissions from a multitude of sources and in a variety of formats. This wealth of data holds great potential to advance CDERs regulatory and scientific work, but the present lack of standardized data creates significant challenges to realizing that potential. The volume and complexity of drug-related information submitted to CDER for regulatory review is creating significant challenges to the Centers ability to efficiently and effectively perform its critical public health mission.
The lack of standardized data affects CDERs review processes by curtailing a reviewers ability to perform integral tasks such as rapid acquisition, analysis, storage and reporting of regulatory data. Improved data quality, accessibility and predictability will give reviewers more time to carry out complex analyses, ask in-depth questions and address late-emerging issues. Standardized data will allow reviewers to increase review consistency and perform evaluations across the drug lifecycle. This will enhance the Centers performance across key drug regulatory functions and ongoing business operations, including pre-market review, post-market safety, oversight of drug quality, and oversight of drug promotion. In accordance with the Office of Management and Budget (OMB) Circular A-119, the FDA will: use voluntary, consensus-based standards development processes in place of government unique standards unless such standards are inconsistent with law or otherwise impractical; advocate to align these standards with existing health information technology initiatives, laws, regulations, and mandates; and promote coordination with other standards currently in use. The projects selected under this funding opportunity must adhere to these principles. OVERARCHING PROGRAM GOAL: The CDER Data Standards Program’s goals are: Support open, consensus-based data standards development Maintain and promote a well-defined data standards governance function Promote the electronic submission of regulatory data using established standards Optimize the regulatory review process to fully leverage data conformed to standards PROGRAM PRIORITIES: The Food and Drug Administration is announcing the availability of cooperative agreements for the development of data concepts and terminology standards to support human drug development and evaluation. The primary objective is to support the development of non-proprietary, consensus-based data standards for use in clinical studies of human drugs and biologics. Projects may focus on the identification of solutions to data standards development and their challenges in areas, such as general clinical and nonclinical study data, specific therapeutic areas, as well as other sections of the regulatory submission (e.g., quality / Chemistry, Manufacturing, and Controls (CMC)). DESCRIPTION: The application must include: An overall program plan describing the approach, process to be used in developing the selected area for standardization, any specific technologies to be utilized and experience with those technologies, and deliverables Definition of scope to be addressed (e.g., use case) during the project period Description of the coordination/collaboration (to achieve consensus) needed to address the area of standardization including by not limited to: engagement of subject matter experts, organizations, standards development organizations, affected stakeholders How the standard being addressed aligns with currently available standards and approach to making the standard publically available Specific Areas of Research Interest: FDA/CDER is specifically interested in projects to develop standardized clinical research concepts and terminology for therapeutic areas with significant drug development pipeline activity, emerging or complex analytical challenges, and/or are of significant public health concern. The list of therapeutic areas with current status is available at: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/ucm287408.htm. |
| Link to Additional Information: | Copy of published RFA |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Gladys Melendez-Bohler
Grants Management Officer/Specialist Phone 240-402-7565 Email:gladys.bohler@fda.hhs.gov |
Related Documents
There are no related documents on this grant.
Packages
| Agency Contact Information: | Gladys Melendez-Bohler Grants Management Officer/Specialist Phone 240-402-7565 Email: gladys.bohler@fda.hhs.gov |
| Who Can Apply: | Organization Applicants |
| Assistance Listing Number | Competition ID | Competition Title | Opportunity Package ID | Opening Date | Closing Date | Actions |
|---|---|---|---|---|---|---|
| 93.103 | ADOBE-FORMS-C | RFA-FD-14-004 | PKG00195924 | Apr 25, 2014 | Jun 16, 2014 | View |
Package 1
Mandatory forms
254499 RR_SF424_2_0-2.0.pdf
254499 PHS398_ResearchPlan_2_0-2.0.pdf
254499 PHS398_CoverPageSupplement_2_0-2.0.pdf
254499 RR_Budget_1_3-1.3.pdf
254499 RR_KeyPersonExpanded_2_0-2.0.pdf
254499 RR_OtherProjectInfo_1_3-1.3.pdf
254499 PerformanceSite_2_0-2.0.pdf
Optional forms
254499 PlannedReport-1.0.pdf
254499 PHS398_CumulativeInclusionReport-1.0.pdf
254499 RR_SubawardBudget30_1_3-1.3.pdf
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