Government Affairs
Overview
Crowell’s Government Affairs Group is smart, strategic, and focused, and our experience is second to none. We do more than open doors to the White House, the halls of Congress and federal and state agencies — for decades, our seasoned professionals have helped clients:
- Create and execute success government affairs strategies to achieve business goals.
- Introduce clients to key U.S. decision makers and educate and advocate on behalf of our client’s business and industry.
- Draft, negotiate, and advocate for new legislation and oppose problematic bills for clients.
- Advocate for clients and track and advise on major government decisions and programs in health care, energy, financial services, infrastructure, technology and other sectors.
- Represent clients in Congressional investigations and help respond to related crises and related issues.
- Provide in-house training to government affairs and business teams.
Insights
Client Alert | 3 min read | 06.26.25
FDA Targets Gene Editing Clinical Trials in China and other “Hostile Countries”
In a somewhat ambiguous press release on Wednesday, June 18, 2025, the Food and Drug Administration (FDA) announced a halt and “immediate review” of new clinical trials where American patients’ cells are sent to China or other “hostile countries” for genetic engineering with the expectation that the cells will be infused back into U.S. patients.[1] A subsequent podcast published by the agency also said that therapies that involved cells that were sent to China for genetic engineering and intended for subsequent infusion into U.S. patients would not be approved going forward. The announcement said that there is “mounting evidence” that some clinical researchers failed to obtain informed consent from trial participants about the international transfer and manipulation of biological material.
Firm News | 3 min read | 06.24.25
Senior DHS Cyber and Emerging Technology Official Matthew F. Ferraro Joins Crowell & Moring
Client Alert | 4 min read | 06.23.25
Selling Electricity to Data Centers or Any End User: Will FERC Regulate You?
Firm News | 3 min read | 06.17.25
Representative Matters
- Assisted Fortune 15 health care company in addressing government affairs issues related to COVID-19, pharmaceutical drugs and medical device supply and logistics.
- Participated in the creation of a multibillion-dollar fund for U.S. victims of terrorism.
- Recovered $500 million for a private equity fund based in Dubai.
- Worked with industry stakeholders to win repeal of a medical device sales tax that was part of the Affordable Care Act.
- Increased funding to provide free vaccines for dependents of US military personnel.
Insights
Client Alert | 3 min read | 06.26.25
FDA Targets Gene Editing Clinical Trials in China and other “Hostile Countries”
In a somewhat ambiguous press release on Wednesday, June 18, 2025, the Food and Drug Administration (FDA) announced a halt and “immediate review” of new clinical trials where American patients’ cells are sent to China or other “hostile countries” for genetic engineering with the expectation that the cells will be infused back into U.S. patients.[1] A subsequent podcast published by the agency also said that therapies that involved cells that were sent to China for genetic engineering and intended for subsequent infusion into U.S. patients would not be approved going forward. The announcement said that there is “mounting evidence” that some clinical researchers failed to obtain informed consent from trial participants about the international transfer and manipulation of biological material.
Firm News | 3 min read | 06.24.25
Senior DHS Cyber and Emerging Technology Official Matthew F. Ferraro Joins Crowell & Moring
Client Alert | 4 min read | 06.23.25
Selling Electricity to Data Centers or Any End User: Will FERC Regulate You?
Firm News | 3 min read | 06.17.25
Insights
COVID-19 and Frustrated Contractors – Understanding the Federal Landscape in 2020 and Beyond
|05.19.20
FederalHealthIT
Auer Deference After Kisor: Alive or “Zombified”?
|04.01.20
ABA Spring 2020: Infrastructure, Vol. 34 No. 4
Government Affairs – A Surprisingly Open Door for Legislation
|02.26.20
Crowell & Moring's Regulatory Forecast 2020
Government Affairs – Congressional Influence on Rulemaking is on the Rise
|02.27.19
Crowell & Moring's Regulatory Forecast 2019
State of Play: Trump's Regulatory Tapestry – Broad Brushstrokes, Wide-Open Spaces, and Major Opportunities
|05.09.17
Crowell & Moring's Regulatory Forecast 2017
Financial Services — Cybersecurity and New Technologies Take Center Stage
|01.19.16
Crowell & Moring's Regulatory Forecast 2016
Regulatory 2016 - The State of Play
|01.19.16
Crowell & Moring's Regulatory Forecast 2016
F.D.A. to Use A.I. in Drug Approvals to ‘Radically Increase Efficiency’
|06.10.25
The New York Times (subscription required)
On the Road: Congressional State of Play
|02.19.25
Crowell & Moring’s Transportation Law: Moving Forward
- |
05.10.16
Crowell & Moring's Government Contracts Legal Forum
'Fair Pay and Safe Workplaces' Rules Head to White House for Final Review
|05.06.16
Crowell & Moring's Government Contracts Legal Forum
- |
02.05.16
Crowell & Moring's Data Law Insights
Technology Coalition tells the President: Encryption Back Doors are a Bad Idea
|05.20.15
Crowell & Moring's Data Law Insights
Supreme Court to Consider Congressionally-Conferred Privacy Breach Standing
|04.29.15
Crowell & Moring's Data Law Insights
Next Generation ACO Model Sets Tone for CMS's Push Toward Value-Based Payment
|03.19.15
Crowell & Moring's Health Law Blog
Cyber Executive Order Continues the Push for Public-Private Partnerships
|02.23.15
Crowell & Moring's Data Law Insights
Professionals
Insights
Client Alert | 3 min read | 06.26.25
FDA Targets Gene Editing Clinical Trials in China and other “Hostile Countries”
In a somewhat ambiguous press release on Wednesday, June 18, 2025, the Food and Drug Administration (FDA) announced a halt and “immediate review” of new clinical trials where American patients’ cells are sent to China or other “hostile countries” for genetic engineering with the expectation that the cells will be infused back into U.S. patients.[1] A subsequent podcast published by the agency also said that therapies that involved cells that were sent to China for genetic engineering and intended for subsequent infusion into U.S. patients would not be approved going forward. The announcement said that there is “mounting evidence” that some clinical researchers failed to obtain informed consent from trial participants about the international transfer and manipulation of biological material.
Firm News | 3 min read | 06.24.25
Senior DHS Cyber and Emerging Technology Official Matthew F. Ferraro Joins Crowell & Moring
Client Alert | 4 min read | 06.23.25
Selling Electricity to Data Centers or Any End User: Will FERC Regulate You?
Firm News | 3 min read | 06.17.25
Insights
Client Alert | 3 min read | 06.26.25
FDA Targets Gene Editing Clinical Trials in China and other “Hostile Countries”
In a somewhat ambiguous press release on Wednesday, June 18, 2025, the Food and Drug Administration (FDA) announced a halt and “immediate review” of new clinical trials where American patients’ cells are sent to China or other “hostile countries” for genetic engineering with the expectation that the cells will be infused back into U.S. patients.[1] A subsequent podcast published by the agency also said that therapies that involved cells that were sent to China for genetic engineering and intended for subsequent infusion into U.S. patients would not be approved going forward. The announcement said that there is “mounting evidence” that some clinical researchers failed to obtain informed consent from trial participants about the international transfer and manipulation of biological material.
Firm News | 3 min read | 06.24.25
Senior DHS Cyber and Emerging Technology Official Matthew F. Ferraro Joins Crowell & Moring
Client Alert | 4 min read | 06.23.25
Selling Electricity to Data Centers or Any End User: Will FERC Regulate You?
Firm News | 3 min read | 06.17.25