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A Cooperative Research and Development Agreement (CRADA) that outlines terms for collaborative research and development activities conducted between the National Institute of Health (NIH) and a designated
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How to fill out COOPERATIVE RESEARCH AND DEVELOPMENT AGREEMENT FOR EXTRAMURAL-PHS CLINICAL RESEARCH

01
Begin by downloading the COOPERATIVE RESEARCH AND DEVELOPMENT AGREEMENT for EXTRAMURAL-PHS CLINICAL RESEARCH form from the official website.
02
Read the instructions carefully to understand the requirements and objectives of the document.
03
Fill in the title of the project at the top of the form.
04
Provide names and contact information for both parties involved in the agreement.
05
Clearly define the scope of research and development including objectives, timelines, and expected outcomes.
06
Outline the roles and responsibilities of each party, including any contributions or resources from both sides.
07
Include details regarding funding, cost-sharing, and budget allocations.
08
Specify the confidentiality terms and conditions to protect sensitive information.
09
Review and confirm compliance with PHS (Public Health Service) regulations and requirements.
10
Obtain signatures from all involved parties to validate the agreement.

Who needs COOPERATIVE RESEARCH AND DEVELOPMENT AGREEMENT FOR EXTRAMURAL-PHS CLINICAL RESEARCH?

01
Academic institutions conducting clinical research.
02
Private research organizations collaborating with government agencies.
03
Healthcare professionals involved in clinical trials.
04
Sponsors or funders looking to formalize research collaborations.
05
Any entity aiming to engage in cooperative research with PHS.
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People Also Ask about

A CRADA provides a way for public and private partners to engage in collaborative research and development with DOE laboratories for the mutual benefit of both parties. Under a CRADA: The Lab and the Partner may share costs or the Partner may pay the 100% of the costs. The Lab and the Partner may elect to own
A CRADA is used when the following circumstances obtain: A cooperative research and development project between a Government scientist and a scientist from the private sector is contemplated. The exchange of material and/or research and development collaboration takes place over a substantial period of time.
Cooperative Research and Development Agreements (CRADAs) CRADAs provide VA with a flexible vehicle to facilitate the transfer of commercially useful technologies to the nonfederal sector. All CRADAs require a completed statement of work (SOW), R&D committee approval, and concurrence from OGC prior to execution.
The process by which knowledge, facilities, or capabilities developed in one place or for one purpose are transferred and utilized in another place for another purpose to fulfill actual or potential public or domestic needs.
Created as a result of the Stevenson-Wydler Technology Innovation Act of 1980, a CRADA allows the U.S. federal government and nonfederal participants to optimize their resources, share technical expertise in a protected environment, share intellectual property emerging from the effort, and advance the commercialization
A non-Federal party may provide funds, in addition to personnel, services, facilities, and equipment to the joint effort.

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The Cooperative Research and Development Agreement (CRADA) for Extramural-PHS Clinical Research is a legal document that facilitates collaboration between the Public Health Service (PHS) and external entities such as academic institutions, private industry, and other organizations for clinical research purposes. It outlines the terms of collaboration, including roles, responsibilities, and the sharing of research findings.
Any institution or organization, including universities, non-profit organizations, and private companies, that engages in cooperative clinical research with the PHS is required to file a CRADA. This includes both the PHS investigators and the external collaborators involved in the research.
To fill out a CRADA for Extramural-PHS Clinical Research, the parties involved must provide detailed information about the research project, including the project title, objectives, funding sources, duration, and the roles of each party. They must also outline the intellectual property rights and how data will be shared. It is recommended to consult legal or administrative support teams to ensure compliance with PHS policies.
The purpose of the CRADA for Extramural-PHS Clinical Research is to promote collaborative research that leverages the strengths of different organizations, facilitates access to resources, and accelerates advancements in medical knowledge and public health. It aims to ensure that research can be conducted effectively while protecting the interests of all parties involved.
The information that must be reported on a CRADA includes details regarding the research project such as its objectives, the roles and contributions of involved parties, financial arrangements, potential conflicts of interest, and agreements on intellectual property rights and data-sharing practices. Regular progress updates may also be required.
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