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The MIT Press and UC Berkeley launch Rapid Reviews: COVID-19

RR:C19 is a new open access, rapid-review overlay journal to combat misinformation in COVID-19 research

Published onJun 29, 2020
The MIT Press and UC Berkeley launch Rapid Reviews: COVID-19

CAMBRIDGE, MA - June 29, 2020—The MIT Press announced today the launch of Rapid Reviews: COVID-19 (RR:C19), an open access, rapid-review overlay journal that will accelerate peer review of COVID-19-related research and deliver real-time, verified scientific information that policymakers and health leaders can use.

Scientists and researchers are working overtime to understand the SARS-CoV-2 virus and are producing an unprecedented amount of preprint scholarship that is publicly available online but has not been vetted yet by peer review for accuracy. Traditional peer review can take four or more weeks to complete, but RR:C19’s editorial team, led by editor-in-chief, Stefano M. Bertozzi, Professor of Health Policy and Management and Dean Emeritus of the School of Public Health at University of California Berkeley, will produce expert reviews in a matter of days.

Using artificial intelligence tools, a global team will identify promising scholarship in preprint repositories, commission expert peer reviews, and publish the results on an open access platform in a completely transparent process. The journal will strive for disciplinary and geographic breadth, sourcing manuscripts from all regions and across a wide variety of fields, including medicine; public health; the physical, biological, and chemical sciences; the social sciences; and the humanities. RR:C19 will also provide a new publishing option for revised papers that are positively reviewed.

Made possible by a $350,000 grant from the Patrick J. McGovern Foundation and hosted on PubPub, an open-source publishing platform from the Knowledge Futures Group for collaboratively editing and publishing journals, monographs, and other open access scholarly content, RR:C19 will limit the spread of misinformation about COVID-19, according to editor-in-chief Bertozzi.

“There is an urgent need to validate—or debunk—the rapidly growing volume of COVID-19-related manuscripts on preprint servers,” explains Bertozzi. “I'm excited to be working with the MIT Press, the Patrick J. McGovern Foundation, and the Knowledge Futures Group to create a novel publishing model that has the potential to more efficiently translate important scientific results into action. We are also working with COVIDScholar, an initiative of UC Berkeley and Lawrence Berkeley National Lab, to create unique AI/machine learning tools to support the review of hundreds of preprints per week.”

“This project signals a breakthrough in academic publishing, bringing together urgency and scientific rigor so the world’s researchers can rapidly disseminate new discoveries that we can trust,” says Vilas Dhar, trustee of the Patrick J. McGovern Foundation. “We are confident the RR:C19 journal will quickly become an invaluable resource for researchers, public health officials, and healthcare providers on the frontline of this pandemic. We’re also excited about the potential for a long-term transformation in how we evaluate and share research across all scientific disciplines.”

On the collaboration around this new journal, Travis Rich, executive director of the Knowledge Futures Group notes, “At a moment when credibility is increasingly crucial to the well-being of society, we’re thrilled to be partnering with this innovative journal to expand the idea of reviews as first-class research objects, both on PubPub and as a model for others.”

Amy Brand, director of the MIT Press sees the no-cost open access model as a way to increase the impact of global research and disseminate high-quality scholarship. “Offering a peer-reviewed model on top of preprints will bring a level of diligence that clinicians, researchers, and others worldwide rely on to make sound judgments about the current crisis and its amelioration,” says Brand. “The project also aims to provide a proof-of-concept for new models of peer-review and rapid publishing for broader applications.”

RR:C19 will publish its first reviews in July 2020 and is actively recruiting potential reviewers and contributors. To learn more about this project and its esteemed editorial board, visit rapidreviewscovid19.mitpress.mit.edu


Media Contacts

Jessica Pellien
Associate Director of Publicity
Fortier Public Relations
[email protected]

Emily Paquin Abbas
Communications Coordinator
The MIT Press
[email protected]

 

About the MIT Press
Established in 1962, the MIT Press is one of the largest and most distinguished university presses in the world and a leading publisher of books and journals at the intersection of science, technology, art, social science, and design. MIT Press books and journals are known for their intellectual daring, scholarly standards, interdisciplinary focus, and distinctive design.

About the UC Berkeley School of Public Health
For 75 years and counting, the UC Berkeley SPH has been dedicated to making a transformative impact on the health of populations through its values of health as a right, strength through diversity, think forward, and impact first. To eliminate inequity and injustice that affects the health and dignity of all people, SPH is committed to radical public health collaborations that challenge conventional thinking, leverage technology, and build bridges between research, public policy, education, and action.

About the Patrick J. McGovern Foundation
The Patrick J. McGovern Foundation is dedicated to improving lives globally with information technology, neuroscience, and AI. The Foundation is the legacy of IDG founder Patrick J. McGovern, who believed in the potential for technology to democratize information, improve the human condition, and advance social good.

About the Knowledge Futures Group
The Knowledge Futures Group, a nonprofit originally founded as a partnership between the MIT Press and MIT Media Lab, builds and sustains technology for the production, curation, and preservation of knowledge in service of the public good.

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Thank you for sharing the announcement regarding the launch of Rapid Reviews: COVID-19 (RR). This innovative journal represents a significant advancement in disseminating verified scientific information, crucial for informed decision-making during the global health crisis. The commitment of the MIT Press, the Patrick J. McGovern Foundation, and the Knowledge Futures Group to accelerating the peer review process through AI demonstrates a forward-thinking approach. The interdisciplinary and global reach ensures a comprehensive understanding of the pandemic, similar to how top recruitment agencies in Pakistan for Saudi Arabia operate across borders. The open access model further enhances the accessibility and impact of critical research findings, fostering trust and collaboration. We look forward to the first reviews in July 2020 and the long-term benefits this journal will bring to the scientific community.

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As a manufacturer of electronic cigarettes (e-cigarettes), vapes, or other Electronic Nicotine Delivery Systems (ENDS), it is crucial to be aware of the regulatory framework imposed by the U.S. Food and Drug Administration (FDA). The FDA oversees various aspects of ENDS, including manufacturing, importation, packaging, labeling, advertising, promotion, sale, and distribution. However, it's important to note that FDA regulations apply to ENDS components and parts, excluding accessories.

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If you engage in any of the following activities related to ENDS, you must comply with the FDA's requirements for manufacturers:

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If you operate as a retailer of ENDS products, it is crucial to understand your role in safeguarding the well-being of consumers, particularly youth, and adhering to FDA regulations. The following resources can assist you in complying with FDA tobacco regulations:

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"This is Our Watch" is a voluntary education program designed to provide resources to tobacco retailers, enabling them to better understand and comply with FDA regulations. By actively participating in this program, retailers play a direct role in protecting young individuals from nicotine addiction and the harmful effects of tobacco use. To safeguard the future generation from tobacco-related diseases, it is essential for tobacco retailers to be well-informed about the rules and regulations.

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For comprehensive information regarding federal rules that retailers must follow, the Retail Sales of Tobacco Products offers valuable insights. This resource provides guidance, regulations, and access to webinars specifically curated for retailers in the tobacco industry. By staying updated with these resources, retailers can ensure compliance and contribute to the health and well-being of their communities.

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If you operate a vape shop that offers services such as mixing or preparing e-liquids containing nicotine or modifying ENDS products, it is important to note that you may be classified as both a manufacturer and a retailer of tobacco products. Consequently, you are required to comply with the regulations outlined for both roles, as mentioned above.

Conclusion

In conclusion, understanding and complying with FDA regulations is crucial for vape manufacturers and retailers involved in the production, distribution, and sale of E-Cigarettes, Vapes, or other ENDS. By adhering to these regulations, you contribute to the safety and well-being of consumers, particularly young individuals. Stay informed, seek guidance when needed, and ensure compliance to navigate the regulatory landscape effectively.

FAQs

1. Are accessories for ENDS devices regulated by the FDA?
No, FDA regulations for ENDS cover components and parts but exclude accessories.

2. What are some examples of regulated components of ENDS?
Regulated components include e-liquids, cartridges, atomizers, batteries, tank systems, flavorings, and more.

3. What should I do if I have specific questions about FDA requirements for small businesses?
You can contact the Office of Small Business Assistance within the FDA's Center for Tobacco Products (CTP) for guidance and answers to your queries.

4. How can vape shops comply with FDA regulations?
Vape shops must adhere to the requirements for both manufacturers and retailers, as they may have legal responsibilities in both capacities.

5. What resources are available for tobacco retailers to understand and comply with FDA regulations?
The "This is Our Watch" program and the Retail Sales of Tobacco Products provide valuable resources, guidance, and webinars for tobacco retailers to ensure compliance with FDA regulations.

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