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This Pre-Solicitation opportunity was posted on February 20, 2018. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Support for Cancer Prevention Agent Development

Closed
N02CN75008-10Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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NAICS: 541690
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City of Delta

POSTED

about 15 hours ago

DEADLINE

in 27 days
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New
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POSTED

about 19 hours ago

DEADLINE

in 15 days
NAICS: 541690
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Growth and Yield Modelling Using MGM
Solicitation # 1070-30/FH27FHQ131
The Ministry of Forests for the Province of British Columbia is issuing a Notice of Intent to direct award a contract for growth and yield modelling using the Mixedwood Growth Model (MGM) to Carolyn Gao. The project involves applying advanced knowledge of the MGM to support modelling analyses and the development of stocking standards for broadleaf, mixedwood, successional, and conifer regeneration and free growing. Key deliverables include proposing changes to competing vegetation criteria for conifer stocking standards, developing algorithms to project stand attributes from free growing survey data, and creating full rotation management regimes focused on timber, wildfire resilience, habitat, and biodiversity. The contract is expected to run from November 1, 2026, to March 31, 2027, with an aggregate value not to exceed 30,000 dollars, exclusive of taxes. The selected contractor must be available to work an average of 10 to 15 hours per week and collaborate closely with the MGM developer. To successfully challenge this direct award, a respondent must possess a graduate degree in forestry or a related discipline, or be a Registered Professional Forester with at least five years of field experience. Additionally, they must demonstrate at least two years of experience applying the MGM within the last five years, experience with boreal or sub-boreal mixedwood stands, and expertise in statistical analysis and the interpretation of growth and yield outputs.
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POSTED

1 day ago

DEADLINE

in 8 days

AI Contract Overview

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Awarded on August 24, 2018, contract HHSN261201800017C designates CCS Associates, Inc., based in San Jose, California, to provide regulatory support for cancer prevention agent development. The total value of the contract is 13,846,650 dollars, covering a maximum period of 60 months. The agreement consists of a base period running from September 30, 2018, to September 29, 2019, valued at 2,653,402 dollars, followed by four optional 12-month terms. These options are valued incrementally from 2,712,613 dollars for the first option up to 2,889,363 dollars for the final term. Performance is conducted at the contractor's place of business, with administrative oversight provided by the contracting office in Rockville, Maryland.

General Info

Agency

N/A

Contract Value

$13,247,902.41

NAICS

541690 - Other Scientific and Technical Consulting Services

Place of Performance

National Cancer Institute 9609 Medical Center Drive, ROCKVILLE, MD, 20852, USA

Set-Aside

SBA

Award Issued Date

Documents

0

No documents available

Documents will appear here when they are available.

AI Contract Breakdown

Uniform Contract Format

No documents to break down

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Timeline

2 updates
PhaseClosed
Posted

Presolicitation

Response Deadline

Deadline has passed

Notice updated

Response deadline changed from Mar 14, 2018 to Apr 13, 2018. The notice description changed.

Notice updated

The notice description changed.

Type Changed

Presolicitation → Solicitation

Submission Closed

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Organization & Contact Information

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AgencyN/A
Contacts2 people available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
Contacts
Yifan YangContracting Officer
Sara M. McLaurinContracting Officer

Full Description

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Note: This synopsis follows a Small Business Sources Sought notice that was released on April 12, 2017 under HHS-NIH-NCI-SBSS-PCPSB-75008-10 THIS IS A NOTICE OF INTENT, NOT A REQUEST FOR PROPOSAL. A SOLICITATION WILL BE ISSUED ON A LATER DATE. Title: Regulatory Support for Cancer Prevention Agent Development Description: The purpose of the acquisition (re-competition) is to provide regulatory services and technical support to the Division of Cancer Prevention (DCP) at the National Cancer Institute (NCI). Technical Support is required to gather, interpret and summarize the vast amount of preclinical and clinical data associated with potential cancer preventive agents. This data is generated by the scientific community and NCI contract labs. Much of this data is used to prepare required reports for FDA review. This contract will prepare and maintain documents required by the Food and Drug Administration (FDA) and other regulatory bodies for clinical trials of investigational agents. Background: The National Cancer Institute (NCI), Division of Cancer Prevention (DCP) has over 40 active clinical trials, 15 trials in development and is the sponsor for approximately 35 INDs (Investigational New Drug Applications). DCPs INDs are located in six Divisions at the FDA. The mission of DCP is to plan and direct cancer prevention research, including testing promising agents in human clinical trials as part of a drug development program. Such testing falls under the purview of regulatory agencies such as the FDA and requires certain documentation for the use of the investigational agent. The collection, preparation, submission and continual update of this documentation is the focus of this acquisition. The current contractor for this acquisition is CCS Associates Inc., 1923 Landings Dr. Mountain View, CA 94043. Technical and Contractual Requirement: The proposed acquisition will involve the following type of activities, further defined in the attached Statement of Work (Attachment 1): 1) Provide regulatory submissions to support the DCP's chemoprevention agent development and clinical research program. 2) Prepare, review, maintain, and track correspondence related to regulatory submission. 3) Provide regulatory support for safety data (adverse event) review, processing, and submission to regulatory agencies and investigators. 4) Maintain electronic and paper files of agreement documents and other documents from pharmaceutical companies. 5) Assist in scheduling, facilitating, and attending meetings to support DCP's regulatory affairs, agent development, and clinical research programs. 6) Manage regulatory documents such as Investigational New Drug Applications (INDs) and Drug Master Files (DMFs) in accordance with regulations, laws, and guidance. 7) Perform regulatory and safety reviews, reporting and advisory activities. 8) Prepare, process and establish a written plan for quality assurance and quality control of all data and procedures. 9) Maintain and enhance standard procedures for information management to support DCP's regulatory affairs. 10) Assist in the transition of the existing contract to the successor contractor. This acquisition will be a total small business set-aside. The Government anticipates that one (1) contract will be awarded with a base period of one year and four one-year option periods. The Product Service Code is R499 and the NAICs Code is 541690; the size standard for this acquisition is $15,000,000. The RFP will be available electronically on or about March 2018 and may be accessed through the FedBizOpps at www.fbo.gov. WE ENCOURAGE ALL RESPONSIBLE SMALL BUSINESS SOURCES, TO SUBMIT A PROPOSAL, WHICH WILL BE CONSIDERED BY THE AGENCY. This notice does not commit the Government to award a contract. No collect calls will be accepted. No facsimile or email transmissions will be accepted. IT IS THE OFFEROR'S RESPONSIBILITY TO MONITOR THE ABOVE-MENTIONED SITE FOR THE RELEASE OF THE SOLICITATION AND ANY AMENDMENTS. Contracting Office Address: 9609 Medical Center Drive Bethesda, Maryland 20852 Primary Point of Contact: Yifan Yang Contracting Officer yifan.yang@nih.gov Phone: 240-276-5282 Secondary Point of Contact: Sara McLaurin Contracting Officer mclaurinsm@mail.nih.gov Phone: 240-276-5488

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