2021 BAA Announcement -BAA 75D301-21-R-71744.pdf
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This broad agency announcement from the Department of Health and Human Services Centers for Disease Control and Prevention solicits concept papers and proposals to improve mine safety and health through research, testing, and development of new technologies. It will consider projects to adapt prototypes, modify technologies for mining applications, analyze technologies or barriers to use, or determine why technologies are not being adopted.
Concept papers are due by January 15, 2021 and full proposals within 30 days of invitation. Awards will fund projects up to $650,000 that improve safety issues like dust exposure, automation, or battery risks. The typical award is $200,000-$300,000. Approximately 6 to 10 awards will be made totaling $2-5 million. Focus areas include issues from the National Academy of Sciences report on dust monitoring, roof bolter automation and dust reduction, and flame arrestors for battery runaways. The announcement will remain open until replaced.
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NIOSH BAA
Announcement
75D301-21-R-71744
2021 Broad Agency Announcement (BAA): Development and Demonstration of Mine Safety and Health Technology
INTRODUCTION
This publication constitutes a Broad Agency Announcement (BAA) by the Department of Health and Human Services, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health (NIOSH), as contemplated in Federal Acquisition Regulation (FAR) 6.102(d)(2). A formal Request for Proposals (RFP), solicitation, and/or additional information regarding this announcement will not be issued. This announcement will remain open until January 15, 2021 or until replaced by a successor BAA. Concept papers must be submitted by January 15, 2021 for funding consideration during fiscal year 2021.
NIOSH will not issue paper copies of this announcement and reserves the right to select for award, all, some or none of the proposals in response to this announcement. NIOSH provides no funding for direct reimbursement of proposal development costs. Technical and cost proposals (or any other material) submitted in response to this BAA will not be returned. It is the policy of NIOSH to treat all proposals as sensitive competitive information and to disclose their contents only for the purposes of evaluation.
Awards under this BAA will consist of firm fixed price contracts. Therefore, proposals submitted as a result of this announcement will fall under the purview of the Federal Acquisition Regulations
(FAR).
I. GENERAL INFORMATION
A. Agency Name:
Centers for Disease Control and Prevention National Institute for Occupational Safety and Health Office of Mine Safety and Health Research 626 Cochrans Mill Road Pittsburgh, PA 15236
B. Research Opportunity Title: Development and Demonstration of Mine Safety and Health Technology
C. Program Name: Office of Mine Safety and Health Research
D. Research Opportunity Number: 75D301-21-R-71744
E. Response Date: This announcement will remain open until January 15, 2021. Concept papers will be accepted from the release of the solicitation through January 15, 2021, 3:00
PM ET. CONCEPT PAPERS SUBMITTED AFTER THE DEADLINE WILL NOT BE
ACCEPTED. Full proposals for concept papers that are found to be technically acceptable will be due within 30 days after notification by the Contracting Officer.
F. Inquiries and Additional Information: Information and specific questions of a technical business nature only will be accepted via email sent to Contracting Officer, Diane Meeder, at the following address: DMeeder@cdc.gov. Include your name and email address on the message. Responses to the email questions will be handled on a first-come basis and generally will be answered within 10 business days.
PHONE CALLS WILL NOT BE ACCEPTED.
Additional information is also available online at the following address:
http://www.cdc.gov/niosh/mining/researchprogram/fundingops.html
G. Research Opportunity Description
The Mine Improvement and New Emergency Response Act of 2006 (MINER Act) permanently established the Office of Mine Safety and Health Research under the direction of an Associate Director, within the National Institute for Occupational Safety and Health. One purpose of this office is to enhance the development of new technology and technological applications, and to expedite the commercial availability and implementation of such technology in mining environments. The MINER Act grants the Office of Mine Safety and Health Research the authority to (1) award competitive contracts and grants to institutions and private entities to encourage the development and manufacture of mine safety equipment and
(2) award contracts to education institutions or private laboratories for the performance of product testing or related work with respect to new mine technology or equipment. This announcement is an opportunity for the award of contracts for enhancing safety in mines.
The primary goal of the MINER Act technology mandate is to improve/increase the use of technology in mines to improve mineworker safety and health, and the intent of this broad agency announcement is to support enabling activities such as technology identification, validation, demonstration, adaptation, and/or commercialization. The Office of Mine Safety and Health Research of NIOSH is soliciting concept papers to conduct research, exploratory development, testing, or evaluations of new technologies to improve mine safety, or to adapt technologies from other industries for application in mining environments. The primary interest of this broad agency announcement is to promote the modification or final development of practical technologies or systems that can be adopted by the mining community in a short period of time. Under this specific solicitation, proposals to conduct theoretical or basic research will not be considered. NIOSH strongly encourages proposals that include collaboration with mining industry partners who understand the reality of the mining environment and can provide insight into mine design requirements and potential commercialization of the technology.
The following examples are presented to further illustrate appropriate submissions under this solicitation beyond the more general guidance listed previously.
1. A safety and/or health technology that is currently in a prototype stage, which will require funding for final development and adaptation to the mining environment. This could include modification of prototypes to account for operation in the challenging underground http://www.cdc.gov/niosh/mining/researchprogram/fundingops.html coal environment, modification to meet permissibility requirements, and/or demonstration of the technology at actual mine sites.
2. A safety and/or health technology that is currently being used in another industry and requires modification to be adapted for mining applications. This could include system redesign, modification to meet permissibility requirements, in-mine testing to establish the efficacy of the technology, and/or demonstration of the technology at mine sites.
3. Analysis of candidate technologies to establish their potential to improve safety and/or health, and/or analyses of barriers to technology application or means of overcoming such barriers.
4. A safety and/or health technology that is fully developed and available for use but is not being adopted by the industry for reasons that require further analysis. This could include developing an initial operational capability by installing the technology in one or more mines for evaluation and/or market analysis to determine the reasons the technology is not being adopted and the changes that would be necessary to make it acceptable to the industry.
5. Analysis of safety and health information in the surveillance area or other work that involves the extraction of useful data for identifying the future technology needs of the mining industry.
Fatality and injury data continue to highlight the need to develop new or improve existing technologies or adapt technologies from other industries to address safety and health issues in surface and underground mines related to the coal, metal, non-metal, and stone, sand, and gravel mining sectors. NIOSH has typically provided a number of topical areas of importance to guide responders in addressing its highest priorities, this solicitation continues that practice as described below. However, NIOSH encourages responders to propose solutions to other health and safety issues that are responsive to our guidelines; these proposals are evaluated under the same criteria as submittals under the focus area and receive equal consideration for funding. Thirty percent of the contracts funded under this program have come from this category of submittals and, in some fiscal years, have made up fifty to seventy percent of the funded proposals.
1. Additional Investigations related to the NAS report “Monitoring and Sampling Approaches to Assess Underground Coal Mine Dust Exposures” In 2016, Congress directed NIOSH to initiate a study by The National Academy of Sciences to “Consider monitoring technologies and sampling protocols used in the United States and in similarly industrialized countries for the control of respirable coal mine dust (RCMD) exposure in underground coal mines; effects of rock dust mixtures and their application on RCMD measurements; and the efficacy of current monitoring technologies and sampling approaches.” The NAS published their report in 20181. In this report the NAS made a series of recommendations. NIOSH funded four proposals in 2019 related to the NAS report recommendations. NIOSH is interested to continue funding additional proposals related to two recommendations from the report:
1 https:/doi.org/10.17226/25111
Recommendation 2: “Conduct studies to evaluate the exposures of miners not wearing CPDMs to ensure that the approach of detecting and mitigating high-exposures for designated occupations reliably results in mitigating high exposures of all worker.” While both the Bureau of Mines and NIOSH have done work in the past in this area, there is interest in a study to establish if compliance sampling of designated occupations is representative of non-sampled miner exposures.
Recommendation 6: “…NIOSH should incorporate appropriate filter media that is compatible with an end-of-shift analyzer for respirable crystalline.” NIOSH is interested in funding work related to filter media compatible with the TEOM used in the ThermoFisher PDM3700 Personal Dust Monitor that could be utilized with the NIOSH field-based silica monitoring technique2.
2. Roof bolter automation and Operator Dust Exposure Reduction
Full roof bolter automation could potentially serve to remove the operators from musculoskeletal disorder (MSD) issues in bolt and mesh handling and eliminate respirable crystalline silica (RCS) exposure when operating downwind of the continuous miner. Roof bolting is a complex process involving the handling of drill steels, roof bolts and plates, and steel mesh. In addition, there are other ground control installations processes completed by the roof bolter operator and machine such as cable bolting and rib bolting.
However, the main entry roof bolting process is repetitive and could be amenable to efforts to automate the process to eliminate physical operator involvement. Solutions to automate this process, in addition to cable bolting and rib bolting, to remove the need for physically handling the roof bolting materials would be beneficial.
The roof bolter operators are also susceptible to over exposure to RCS dust, especially when downwind of the continuous miner (CM). The current method to reduce this exposure is to regulate the roof bolter operation to only 40 ft. of operation downwind of the miner per shift. The canopy air curtain is also a viable control to reduce operator exposure to RCS. However, its protection has been shown to be variable. Solutions to improve the canopy air curtain protection and/or other solutions to reduce operator exposure downwind of the miner are encouraged.
3. Development of a purpose-built flame or detonation arrestor for li-ion battery thermal runaway Mining equipment powered by li-ion batteries is being developed for use in gassy mines.
Li-ion batteries susceptible to thermal runaway may produce pressurized explosions when
2 https://www.cdc.gov/niosh/mining/researchprogram/projects/project_advancingexposuremonitoring.html https://www.cdc.gov/niosh/mining/researchprogram/projects/project_advancingexposuremonitoring.html confined within sealed enclosures such as explosion proof or flame proof enclosures3.
There is a need for venting of thermal runaway gases to relieve excessive overpressures within the explosion proof or flame proof enclosure while ensuring that ignition of an external explosive mine atmosphere does not occur. Pressure-relieving flame arrestors for enclosures used in gassy mines were designed for arresting methane-air or hydrogen-air ignitions as opposed to thermal runaway gases. Solutions are sought to develop flame or detonation arrestors sufficient for quenching li-ion battery thermal runaway gases released from enclosures, along with supporting test data, test criteria and other information used to determine sufficiency of the arrestor, to prevent mine explosions.
4. Big data analytics and machine learning techniques As fatalities and other severe incidents (i.e., lagging indicators) decrease, the mining industry needs a more proactive approach to risk management that focuses on using Health and Safety (H&S) leading indicator data to help identify, predict, and control risks, Some examples of leading indicator data may include near miss incidents, risk assessments, safety audits, behavioral observations, knowledge assessments, workplace exams, injuries, citations, and worker compensation data from insurance companies or federal websites.
Other sources of data may include data from mine monitoring/tracking systems, equipment operation logs, etc. The objective of this research is to identify and/or improve quantification of safety and health risks through the use big data analytics and machine learning techniques on large datasets. Research questions to be answered may include topics such as “What machine learning techniques or methods can be used to analyze safety big data in the mining industry?” and “What H&S outcomes (i.e. risks) can be predicted using available H&S leading indicator data?” The goal will be to develop machine learning model(s) to accomplish the objective, and at a minimum answer the two proposed research questions.
5. Intrinsically safe devices NIOSH has identified a number of products that have either 1) been approved as intrinsically safe under IEC or other authorities or 2) had MSHA approval but, as electronic components become unavailable or technologically obsolete, are no longer available.
NIOSH would like to facilitate an introduction or return of these products or similar offerings to market. (Note that NIOSH cannot pay for the cost of the approval, but only for design and prototype work.) The examples below are for illustrative purposes only.
• Intrinsically safe camera for the utilization of Helmet-CAM technology.
• Portable, intrinsically safe logging anemometer for use in evaluating engineering controls in underground coal mining.
3 Dubaniewicz TH (2020) Thermal Runaway Pressures of Iron Phosphate Li-Ion Cells within Sealed Enclosures.
Presentation to the Global Mining Guidelines Group. https://www.youtube.com/watch?v=JdGIG0qb4Jg https://www.youtube.com/watch?v=JdGIG0qb4Jg
• Permissible PPE alternative for dust exposure utilizing a powered air purifying respirator (PAPR).
• Development of an MSHA approved light scattering instantaneous dust monitor, similar to the previously available Personal DataRAM pDR-1000 Monitor.
• Permissible Electronic Surveying Equipment such as a Total Station.
• Miniature Dataloggers, similar to the Campbell Scientific Model 21X.
The development of products for permissibility should also include technological enhancements to improve performance, reduce the size of the product for better field adaptability, and/or decrease the cost to improve the acceptance of the product in the mining industry.
H. Instrument Type(s) and Period of Performance - Awards will take the form of contracts.
Work that will be completed in 24 to 36 months or less is desired under this solicitation but is not a requirement; projects requiring up to 48 months will be considered.
II. AWARD INFORMATION
NIOSH plans to make awards that represent the best value to the Government in accordance with the evaluation criteria. NIOSH is seeking participants for this program that are capable of developing and demonstrating the technologies required to achieve the goals described in this announcement.
1. Total amount of funding the program office expects to award through the announcement:
• Approximately $2M to $5M for the duration of this BAA.
2. Anticipated number and estimated value of awards:
• NIOSH estimates that the typical contract award under this solicitation will be between $200,000 to $300,000, although proposals will be considered up to a ceiling of $650,000. Proposals submitted in excess of the $650,000 ceiling will not be evaluated nor considered for funding. It is estimated that approximately 6 to 10 awards will be made.
3. Anticipated award types:
• The contracts will be Firm Fixed Price. NIOSH will not issue grants, cooperative agreements, or other transaction agreements under this BAA.
III. ELIGIBILITY INFORMATION
All potential applicants that meet the requirements of the application and submission deadlines are eligible.
IV. APPLICATION AND SUBMISSION INFORMATION
A. Application and Submission Process
Offerors must submit a Concept Paper prior to submitting a Full Proposal. NIOSH will evaluate the Concept Papers and the CDC Contracting Officer will provide feedback via email to the Offerors for those Concept Papers that will move forward to a full proposal. Full Proposals will be solicited from Concept Papers that are of “particular value” in fulfilling the goals of the Broad Agency Announcement. However, any such request for a Full Proposal submission does not assure a subsequent contract award. The Full Proposals must provide detailed technical and cost information as outlined herein to support the scope of the proposed effort. Full Proposals will be evaluated, and a determination made for contract awards. Full proposals not funded in the current fiscal year may be held over for funding consideration in the following fiscal year, with the approval of the offeror.
B. Content and Format of Concept Papers/Full Proposals
The proposal submissions will be protected from unauthorized disclosure in accordance with FAR 15.207, applicable law, and regulations. Offerors are expected to appropriately mark each page of their submission that contains proprietary information.
General Formatting Requirements (Concept Papers and Full Proposals)
1. Paper Size - 8.5 x 11-inch paper
2. Margins - 1 inch, all
3. Spacing – 1.15 spacing
4. Font - Times New Roman, 12 point
5. Copies - One (1) original and five (5) additional hard copies.
6. Electronic file submission – Files must be submitted as a MS Word document with the exception of the cover pages for the Technical and Cost Proposals, which may be a pdf or similar format (including Word) containing the required signatures.
Concept Paper Content (not to exceed 10 pages excluding the cover page, concept papers exceeding the 10 page limit may not be evaluated)
1. Cover Page: A separate cover page shall be labeled "CONCEPT PAPER," and shall include the BAA number, proposed title, Offeror’s administrative and technical points of contact, with telephone numbers, fax numbers, mailing and email addresses, total cost of the concept, period of performance, and corresponding focus area (if applicable) that is listed in the solicitation, and shall be signed by an authorized officer.
2. Abbreviated Statement of Work:
DO NOT INCLUDE ANY PROPRIETARY DATA OR MARKINGS IN THE STATEMENT
OF WORK (SOW). The abbreviated SOW must be provided that clearly describes the objectives, scope of work, and the technical approach.
The following SOW format shall be used:
a. Title of Project: Provide descriptive title that reflects the proposed effort.
b. Synopsis of the Technical Approach. This section shall include the Problem Statement or Focus Area and identify specifically what mine safety issue or focus area this proposed technology development is attempting to address.
i. Background (no more than one page): The background section should provide a clear and brief description of the relevance of the proposed effort and discuss the technology that will be proposed in general, non-technical terms. The background section should address four specific areas: (1) provide an assessment of the current body of knowledge, (2) the status of related industry product developments, and (3) the remaining steps that are needed to facilitate a commercially viable and available solution for the safety and health issue identified in the proposal; this should include (4) supporting evidence that the proposed work represents the next logical step in arriving at a solution.
ii. Briefly describe the enabling technology that is being proposed and how this technology will be used to solve the issue designated in the problem statement.
iii. Define the state of readiness of the enabling technology and what is needed to bring the proposed technology to the level of development necessary to solve the designated problem.
iv. Identify any known or perceived barriers to the implementation of this technology due to the uniqueness of the mining environment or statutory regulations.
c. Objective: A brief and succinct statement of what will be done relevant to the problem statement and the expected outcome.
d. Scope of Work (no more than five pages): The scope of work should provide a brief and clear description in non-technical terms as much as possible and should identify the major steps that will be undertaken to achieve the proposed outcome. The scope of work should address the following areas:
i. Briefly describe the current state of the technology.
ii. Address the issues expressed in the background section and how the proposed technology will be developed to solve the problem.
iii. Briefly describe the specific tasks and phases of the work.
iv. Specify the period of performance for the total effort and each task or phase.
v. Milestones, schedule and decision points regarding the development of the technology including rough estimates of cost for each year, task and phase of the effort and total cost.
vi. Briefly identify the required steps to overcome the perceived barriers to the implantation of this technology.
e. Deliverables (no more than two pages): Provide a summary of the deliverables including:
i. Monthly technical reports.
ii. Monthly financial progress reports.
iii. Milestone reports.
iv. Draft Final and Final report. (Note: Time must be included in the schedule for the Government to review the Draft Final report, typically 30 days)
v. All data collection and analysis protocols as applicable.
vi. A prototype of the developed product (optional).
f. Key Personnel (no more than two pages): A brief summary of the key personnel including: a listing of key personnel with a short summary of qualifications.
Full Proposal Content
1. Volume 1: Technical Proposal - Each section of the Technical Proposal must start on a new page. DO NOT PROVIDE COMMERCIAL PRODUCT ADVERTISING
BROCHURES.
• Cover Page: A separate cover page must include the words "TECHNICAL
PROPOSAL" and the following:
o BAA number;
o Title of Proposal;
o Identity of prime Offeror and complete list of collaborators and subcontractors, if applicable;
o Technical contact (name, address, phone/fax, email and mailing address);
o Administrative/business contact (name, address, phone/fax, email and mailing address), and;
o Period of performance.
• Table of Contents
• Statement of Work (not to exceed 15 pages): DO NOT INCLUDE ANY
PROPRIETARY DATA OR MARKINGS IN THE STATEMENT OF WORK
(SOW). A SOW must be provided that clearly describes the objectives, scope of work, and the technical approach. Proposals must include a severable, unclassified, self-standing SOW without any proprietary restrictions. It is anticipated that the proposed SOW may be incorporated as an attachment to the resultant award instrument. The Government also reserves the right to modify the proposed SOW based on clarification sessions with the Offer prior to the agreement award. The following SOW format shall be used:
o Title of Project: Provide descriptive title that reflects the proposed effort.
o Problem Statement or Focus Area: Identify specifically what mine safety issue or focus area this proposal is attempting to address.
o Background: The background section should provide a clear indication of the relevance of the proposed effort and discuss the technology that will be proposed in general, non-technical terms. The background section should address four specific areas:
• Provide an assessment of the current body of knowledge, the status of related industry product developments, and the remaining steps that are needed to facilitate a commercially viable and available solution for the safety and health issue identified in the proposal.
This should include supporting evidence that the proposed work represents the next logical step in arriving at a solution.
• Identify the enabling technology that is being proposed and how this technology will be used to solve the issue designated in the problem statement.
• Identify the state of readiness of the enabling technology and what is needed to bring the proposed technology to the level of development necessary to solve the designated problem.
Identify any known or perceived barriers to the implementation of this technology due to the uniqueness of the mining environment or statutory regulations.
o Objective: A succinct statement of what will be done relevant to the problem statement and the expected outcome if this effort is funded.
o Scope of Work: The scope of work should provide a clear description in non-technical terms as much as possible and should also expand on the project objectives and of the major steps that will be undertaken to achieve the proposed outcome. The scope of work should address the following areas:
• Current state of the technology.
• Specific information addressing the issues expressed in the background section pertaining to how the technology will be developed to solve the problem.
• Describes the specific tasks and phases of the work. When optional tasks or phases are offered beyond the base proposal, they must be separately and clearly identified as optional tasks and phases.
• Specify the period of performance for the total effort and each task or phase (including optional tasks or phases).
• Milestones and schedule of events that can be used as progress metrics and decision points regarding the development of the technology.
• Identify the required steps to overcome the perceived barriers to the implantation of this technology.
• Potential paths or avenues to commercialization.
• References: Describes any reference materials that may be relevant to the work being performed.
• Deliverables and Reporting Schedule: Detailed summary of deliverables to be provided under the contract. Describe any reporting requirements including content and format, including Delivery and ownership of products hardware produced under this effort. Also required is delineation of documentation including but not limited to the following:
o Monthly technical reports.
o Milestone reports.
o Draft Final and Final Report (Note: Time must be included in the schedule for the Government to review the Draft Final report, typically 30 days. Five copies of the final report are required.).
o All data collection and analysis protocols as applicable.
o A prototype of the developed product (optional).
At a minimum, a final technical report is required and is to be delivered in both hard copy and electronic (Word or PDF) format. The final report must be 508 compliant. If the final report contains proprietary information, a second version of the report must be prepared and submitted in both hard copy and electronic format that is suitable for public release.
The contractor shall submit a completed HHS Section 508 Checklist to assist the Government in determining that the Final Report is Section 508 compliant. In addition, the contractor shall submit the result of running the accessibility self-check in either Word or PDF format. Additional information is available on the HHS Section 508 website (https://www.hhs.gov/web/section-508/index.html and https://www.hhs.gov/web/section-508/making-files-accessible/index.html)
• Special Considerations: Information that does not fit neatly or logically into one of the other sections.
• Carry-over Acknowledgement and Conditions: State if the offeror approves the carry-over of the Full Proposal, if not selected for funding under this solicitation, for consideration during the next fiscal year. Identify any conditions or issues associated with that action.
• Government Furnished Property: Document any government furnished property that is required to complete the Scope of Work.
• Assertion of Data Rights (not to exceed 1 page): Include here a summary of any proprietary rights to preexisting results, prototypes, or systems supporting and/or necessary for the use of the research, results, and/or prototype. Any rights made in other parts of the proposal that would impact the rights in this section must be cross-referenced. If there are proprietary rights, the Offeror must explain how these affect its ability to deliver subsystems and toolkits for integration. Additionally, Offerors must explain how the program goals are achievable in light of these proprietary and/or restrictive limitations. If there are no claims of proprietary rights in preexisting data, this section shall consist of a statement to that effect.
• Resource Sharing Plan(s)
HHS/CDC policy requires that recipients of contract awards make research resources and data readily available for research purposes to qualified individuals within the scientific community after publication.
CDC requires awardees for projects and programs that involve the collection or generation of data with federal funds to develop, submit and comply with a Data Management Plan (DMP) for each collection or generation of public health data undertaken as part of the award and, to the extent appropriate, provide access to and archiving/long-term preservation of collected or generated data.
https://www.hhs.gov/web/section-508/index.html https://www.hhs.gov/web/section-508/making-files-accessible/index.html
HHSAR Provision, 352.239-73: Electronic and Information Technology Accessibility Notice
(a) Section 508 of the Rehabilitation Act of 1973 (29 U.S.C. 794d), as amended by the Workforce Investment Act of 1998 and the Architectural and Transportation Barriers Compliance Board Electronic and Information (EIT) Accessibility Standards (36 CFR part 1194), require that when Federal agencies develop, procure, maintain, or use electronic and information technology, Federal employees with disabilities have access to and use of information and data that is comparable to the access and use by Federal employees who are not individuals with disabilities, unless an undue burden would be imposed on the agency. Section 508 also requires that individuals with disabilities, who are members of the public seeking information or services from a Federal agency, have access to and use of information and data that is comparable to that provided to the public who are not individuals with disabilities, unless an undue burden would be imposed on the agency.
(b) Accordingly, any offeror responding to this solicitation must comply with established HHS EIT accessibility standards. Information about Section 508 is available at http://www.hhs.gov/web/508. The complete text of the Section 508 Final Provisions can be accessed at http://www.access-board.gov/sec508/standards.htm.
(c) The Section 508 accessibility standards applicable to this contract are:
205 WCAG 2.0 Level A & AA Success Criteria 302 Functional Performance Criteria 502 Inoperability with Assistive Technology 503 Applications 504 Authoring Tools 602 Support Documentation
603 Support Services
In order to facilitate the Government's determination whether proposed EIT supplies meet applicable Section 508 accessibility standards, offerors must submit an HHS Section 508 Product Assessment Template, in accordance with its completion instructions. The purpose of the template is to assist HHS acquisition and program officials in determining whether proposed EIT supplies conform to applicable Section 508 accessibility standards. The template allows offerors or developers to self-evaluate their supplies and documentation detail - whether they conform to a specific Section 508 accessibility standard, and any underway remediation efforts addressing conformance issues. Instructions for preparing the HHS Section 508 Evaluation Template are available under Section 508 policy on the HHS Web site http://hhs.gov/web/508.
In order to facilitate the Government's determination whether proposed EIT services meet applicable Section 508 accessibility standards, offerors must provide enough information to assist the Government in determining that the EIT services conform to Section 508 accessibility standards, including any underway remediation efforts addressing conformance issues.
(d) Respondents to this solicitation must identify any exception to Section 508 requirements. If a offeror claims its supplies or services meet applicable Section 508 accessibility standards, and it is later determined by the Government, i.e., after award of a contract or order, that supplies or services delivered http://www.hhs.gov/web/508 http://www.access-board.gov/sec508/standards.htm http://www.access-board.gov/sec508/standards.htm http://hhs.gov/web/508 do not conform to the accessibility standards, remediation of the supplies or services to the level of conformance specified in the contract will be the responsibility of the Contractor at its expense.
(e) Electronic content must be accessible to HHS acceptance criteria. Checklist for various formats are available at http://508.hhs.gov/, or from the Section 508 Coordinator listed at https://www.hhs.gov/web/section-508/additional-resources/section-508-contacts/index.html. Materials that are final items for delivery should be accompanied by the appropriate checklist, except upon approval of the Contracting Officer or Representative.
Data Management Plan
Consistent with the terms of and activities expected under the funding opportunity announcement (FOA), as applicable, awardees must develop and submit a DMP generally during the project planning phase, but in any event, prior to the initiation of generating or collecting public health data. Accordingly, the DMP may be evaluated during the application, study proposal, or project review process or during other times in the project period. For FOAs that involve already defined projects which include data collection or generation at the time of application, applications submitted without the required DMP may be deemed non-responsive for award. For FOAs where CDC specifies that submission of the DMP is deferred to a later period, funding restrictions may be imposed pending submission and evaluation of the DMP. For awards where data collection or generation activities may become necessary during the project period, DMPs will be required to be submitted and evaluated during the project period of the award. In all instances described above, the reviewing officials have to approve an acceptable DMP.
Costs associated with developing and implementing a DMP, including costs of sharing, archiving and long-term preservation, may be included in the cost proposal.
A DMP for each collection and/or generation of public health data funded by this award, as applicable, should include the following information:
•A description of the data to be collected or generated in the proposed project;
•Standards to be used for the collected or generated data;
•Mechanisms for or limitations to providing access to and sharing of the data (include a description of provisions for the protection of privacy, confidentiality, security, intellectual property, or other rights). This section should address access to identifiable and de-identified data (see below for additional information about access);
•Statement of the use of data standards that ensure all released data have appropriate documentation that describes the method of collection, what the data represent, and potential limitations for use; and •Plans for archiving and long-term preservation of the data, or explaining why long-term preservation and access are not justified. This section should address archiving and preservation of identifiable and de-identified data (see below for additional information regarding archiving).
http://508.hhs.gov/ https://www.hhs.gov/web/section-508/additional-resources/section-508-contacts/index.html
Access to and Archiving of the Data
Awardees whose terms of award do not include submitting data to CDC are expected to plan and prepare for access to and archiving/long-term preservation of collected and/or generated data within the funding period, as set forth below. The final version of a collected and/or generated data set intended for release or sharing should be made available within thirty (30) months after the end of the data collection or generation, except surveillance data which should be made accessible within a year of the end of a collection cycle. In addition, awardees should ensure the quality of data they make accessible and seek to provide the data in a nonproprietary format. Awardees who fail to release public health data in a timely fashion may be subject to procedures normally used to address lack of compliance consistent with applicable authorities, regulations, policies or terms of their award.
For public use de-identified (removal of sensitive identifiable or potentially identifiable information) datasets, an accompanying data dictionary, and other documentation relevant to use of the data set should be deposited in a sustainable repository to provide access to the data. Data that cannot be de-identified can be provided on request under a data-use agreement.
Awardees will be required to inform the appropriate CDC point-of-contact identified in the award via an update to their DMP of the location of the deposited data. The DMP is a living document that should be updated throughout the life cycle of data.
For data underlying scientific publication, awardee should make the data available coincident with publication of the paper, unless the data set is already available via a release or sharing mechanism. At a minimum, release of the data set should consist of a machine-readable version of the data tables shown in the paper.
Requirements set forth in this policy are not intended to conflict with or supersede applicable contract regulations related to agency access to awardee data and records.
Offerors should include a detailed DMP in their technical proposal, as applicable.
The DMP should be developed during the project planning phase prior to the initiation of collecting or generating public health data and will be submitted with the technical proposal. The submitted DMP will be evaluated for completeness and quality at the time of submission.
The DMP should include, at a minimum, a description of the following:
• Type of data to be produced in the proposed project;
• Mechanisms for providing access to and sharing of the data (including provisions for the protection of privacy, confidentiality, security, intellectual property, or other rights);
• Use of data standards that ensure all released data have appropriate documentation that describes the method of collection, what the data represent, and potential limitations for use; and
• Plans for archiving and long-term preservation of the data, or explaining why long-term preservation and access are not justified.
Full proposals submitted without the required DMP, as applicable, may be deemed ineligible for award unless submission of DMP is deferred to a later period depending on the type of award, in which case, funding restrictions may be imposed pending submission and evaluation.
• Qualifications (not to exceed 5 pages): A discussion of previous accomplishments and work in this, or closely related areas, and the qualifications of the investigators. Key personnel resumes shall be attached to the proposal and will not count toward the page limitations.
• Management Approach (not to exceed 1 page): A discussion of the overall approach to the management of this effort, including brief discussions of the total organization, use of personnel, project/function/subcontractor relationships, government research interfaces, and planning, scheduling and control practice.
Identify which personnel, collaborators, and subcontractors (if any) will be involved. Include a description of the facilities that are required for the proposed effort with a description of any government furnished equipment, hardware, software, or information required, by version and/or configuration (Refer to Section VII). Identify any planned collaborations with mining industry partners, including the nature of the collaboration.
2. Volume 2: Cost Proposal - The Cost Proposal shall consist of a cover page and two parts. Part 1 will provide a detailed cost breakdown of all costs by cost category and by calendar/fiscal year. Part 2 will provide a cost breakdown by task/sub task using the same task numbers in the Statement of Work. Optional phases or tasks, if proposed, must be separately priced.
• Cover Page: The use of the SF 1411 is optional. The words "COST PROPOSAL" should appear on the cover page in addition to the following information:
o BAA number;
o Title of Proposal;
o Identity of prime Offeror and complete list of subcontractors, if applicable;
o Technical contact (name, address, phone/fax, email and mailing address);
o Administrative/business contact (name, address, phone/fax, email and mailing address);
o Duration of research and demonstration tasks, o Summary statement of proposed costs, and;
o Cognizant DCAA and DCMA point of contact, address, phone/fax/ and email, if applicable.
• Part 1: For proposal pricing purposes, Offerors should assume a contract start date of September 1, 2021. Part 1 should include the detailed breakdown of all costs by cost category and by calendar/fiscal year. When options are contemplated, options must be separately identified and priced by task/subtask corresponding to the same task numbers in the Statement of Work. Please include:
o Direct Labor - Individual labor category or person, with associated labor hours and unburdened direct labor rates;
o Indirect Costs - Fringe benefits, overhead, G&A, COM, etc. (Must show base amount and rate). Please note: Tuition reimbursement is not an allowable expense for these types of contracts and should not be included in the cost proposal;
o Proposed Contractor Acquired Equipment, such as computer hardware, for proposed research projects should be specifically itemized with costs or estimated costs. An explanation of any estimating factors, including their derivation and application, shall be provided. Please include a brief description of the Offeror’s procurement method to be used;
o Travel - Number of trips, number of days per trip, departure and arrival destinations, number of people, etc. Note that, if funded, travel will be a separate line item in the contract and itemized on all billings;
o Subcontract - A cost proposal as detailed as the Offeror’s cost proposal must be submitted by the subcontractor. The subcontractor's cost proposal can be provided in a sealed envelope with the Offeror’s cost proposal or will be requested from the subcontractor at a later date;
o Consultant - Provide consultant agreement or another document that verifies the proposed loaded daily/hourly rate;
o Materials should be specifically itemized with costs or estimated costs. An explanation of any estimating factors, including their derivation and application, shall be provided. Please note that 5 bound hard copies of the final report will be required by NIOSH and are to be included in the Proposal cost. Please include a brief description of the Offeror’s procurement method to be used;
o Other directs costs, and;
o Fee/profit including fee percentage.
o Offerors are to provide any current Forward Pricing Rate Agreements in effect at the time of the proposal submission.
• Part 2: Cost breakdown by task/subtask using the same task numbers in the Statement of Work. This should include the individual labor category or person, with associated labor hours to permit an evaluation of the required effort. When optional tasks or phases are offered beyond the base proposal, they must be separately identified and priced by task/subtask corresponding to the same task numbers in the Statement of Work. Included in this section shall be a proposed payment schedule, linked to the cost breakdown, deliverables, and milestones.
**Subcontracting Plan: An HHS Small Business Subcontracting Plan is required if the estimated cost of the contract may exceed $750,000 ($1,500,000 for construction) (Note: This requirement does not apply to small business concerns.)
C. Significant Dates and Times
This announcement will remain open until January 15, 2021. Offerors are responsible for submitting concept papers or proposals, and any modification, or revisions, so as to reach the Government office designated in the solicitation by the time specified in the solicitation.
1. Submission of Concept Papers: Concept papers must be received prior to 3:00 PM ET local on January 15, 2021. Any concept papers submitted after 3:00 pm ET local will not be accepted. Almost every year concept papers are rejected based on a late submittal, often just by minutes – this criterion applies without exception.
2. Submission of Proposals: Full proposals for concept papers that are found to be technically acceptable will be due within 30 days after notification by the Contracting Officer. The proposals must be received prior to 3:00 PM ET local on the date specified by the Contracting Officer.
3. Method of submission: Concept papers and full proposals can be submitted electronically via email or by the regular mail (see item 5 below for the addresses). Proposals sent via email must be time stamped by the time indicated in item 2 above (Note: the email date and time becomes the official "time stamp" for electronic submissions.). Electronic files must be submitted as a MS Word document with the exception of the cover page, which may be a pdf or similar format (including Word) containing the required signatures.
4. Information for Electronic Mail (Email) Concept Papers or Proposals
a. Definition. “email concept paper or proposal,” as used in this provision, means a concept paper or proposal, revision or modification of a concept paper or proposal, or withdrawal of a concept paper or proposal that is transmitted to and received by the Government via computers utilizing electronic mail. This does not include facsimile concept papers or proposals which are prohibited for this solicitation.
b. Offerors may submit email concept papers or proposals as responses to this solicitation. Email concept papers or proposals are subject to the same rules as paper concept papers or proposals.
c. If any portion of an email concept paper or proposal received by the Contracting Officer is unreadable to the degree that conformance to the essential requirements of the solicitation cannot be ascertained from the document—
i. The Contracting Officer immediately shall notify the offeror and permit the offeror to resubmit the proposal;
ii. The method and time for resubmission shall be prescribed by the Contracting Officer after consultation with the offeror; and
iii. The resubmission shall be considered as if it were received at the date and time of the original unreadable submission for the purpose of determining timeliness, provided the offeror complies with the time and format requirements for resubmission prescribed by the Contracting Officer.
5. The Government reserves the right to make award solely on the email concept paper or proposal. However, if requested to do so by the Contracting Officer, the apparently successful offeror promptly shall submit the complete original signed concept paper or proposal.
6. Late submissions: Any proposal, modification, or revision received at the Government office designated in the solicitation after the exact time specified for receipt of offers is “late” and will not be considered unless there is acceptable evidence to establish that it was received at the Government installation designated for receipt of offers and was under the Government’s control prior to the time set for receipt of offers.
7. Address for the Submission of Concept Papers and Full Proposals:
Diane Meeder Contracting Officer Centers for Disease Control and Prevention 626 Cochrans Mill Road, Building 140 Pittsburgh, PA 15236-0070
Email: DMeeder@cdc.gov Phone: 412-386-4412
***Due to COVID-19, Electronic Copies are Requested***
V. EVALUATION INFORMATION
A. Evaluation Criteria
Concept Papers and Full Proposals will be evaluated using the following criteria. Past performance for all Offers recommended for an award will be reviewed—a satisfactory performance history is required for funding.
The Government will use the six (6) factors listed below in descending order to make a “best value” determination. Criterion 1-3 are of equal value but individually greater than criterion 4, Criterion 4-5 are of equal value but individually greater than criterion 6. Criterion 6 is of less value individually than criterions 1-5.
1. The proposed work directly addresses (1) a significant health and safety issue in the industry with (2) potential contribution and relevance to the NIOSH Mining Program mission.
2. The overall scientific and technical merit of the proposed work outweighs potential risks.
3. The qualifications of the project team, the Offeror's capabilities, and collaboration with the mining industry are adequate for achieving the proposed work.
4. The proposed work that will be used to address the identified issue is appropriate, innovative, feasible, achievable, and adequate. For proposals that involve generation or collection of public health data, this will include the Data Management Plan (DMP, as defined previously in this solicitation).
5. The proposed work represents a logical, incremental step forward towards developing a commercial product or identifying the need for specific commercial products.
mailto:DMeeder@cdc.gov
6. The…
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