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BIS Considers Export Controls on Neurotechnology and Adds New Controls on Genetic Sequencing Software and Intrusion Software

November 9, 2021

by Lawrence Ward, Dave Townsend, and T. Augustine Lo

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The U.S. Commerce Department’s Bureau of Industry and Security (“BIS”) has said it is contemplating new export controls on certain neurotechnology items and has adopted new controls on genetic sequencing software and intrusion software in a series of announcements.  Under the Export Administration Regulations (“EAR”), BIS imposes export controls on an item-specific basis with export license requirements applying on a country-by-country basis, depending on the national security and foreign policy concerns associated with the items.  An export under the EAR includes actual release or shipment of an item from the United States to another country but also includes providing controlled technology or source code to foreign persons, including employees of businesses, in the United States.

Companies whose operations involve neurotechnology, genetic sequencing software or intrusion software should examine these new export controls to see if export license requirements may apply to provide such newly-controlled software or technology to non-U.S. destinations or to foreign persons in the United States.

Potential Neurotechnology Controls.

On October 25, BIS announced that it is considering new export controls on Brain Control Interface (“BCI”) hardware and technology.  In its advanced notice of public rulemaking (“BCI Notice”), BIS asks for public comments on the scope and extent of these potential controls and whether they should be aligned with export controls implemented by international allies.  Public comments are due to BIS on December 10, 2021.  BIS has posed a series of questions for public comment (see below).  BIS states that it seeks to identify whether BCI could provide U.S. adversaries with “a qualitative military or intelligence advantage.”  BIS defines BCI as a “direct communication pathway between an enhanced or wired brain and an external device” that can translate commands to control machines, communicate with other humans, or assess or enhance human functioning.

Although BIS does not yet propose any specific export controls on BCI, it seems likely the BCI Notice is intended to result in the creation of such BCI export controls in the near future.  BIS issued the BCI Notice under the Export Control Reform Act of 2018 (“ECRA”), which directs BIS to establish new export controls on emerging and foundational technologies. BIS had originally requested public comments on what items should be considered within “emerging technologies” in November 2018 and specifically identified BCI as a potential emerging technology that is essential to U.S. national security.  In response, BIS received 13 comments that discussed BCI. Most of the comments expressed concern over potential BCI export controls harming U.S. business interests (e.g., in artificial intelligence for automobiles or by providing an advantage to non-U.S. businesses that may not be subject to such BCI controls).

BIS therefore seems intent on creating some form of BCI export controls, although it is too early in the federal rulemaking process to predict what those controls ultimately will look like.  However, BIS has posed a series of questions for public comment and response:

(1)  What specific uniform standards for BCI technology would need to be adopted to ensure their application on a global basis (i.e., as international standards for BCI technology)?

(2)  Where does the development of BCI in the United States stand with respect to other countries (e.g., is the United States on the forefront of BCI technology development)?

(3)  Is BCI technology currently available for commercial use in certain foreign countries and, if so, where and for what specific purposes (e.g., have foreign companies already developed devices or chips for specific commercial applications)?

(4)  Has the current stage of development with respect to invasive and/or non-invasive BCI technology reached the point at which such technology is ready for commercial production and use?

(5)  Is the main progress with respect to non-invasive brain signal sensors being made in terms of real-time algorithms designed to transform neural signals into commands (i.e., what is developing faster: “software” (algorithms) or hardware (sensors))?

(6)  What impact would the establishment of export controls on BCI technology have on U.S. technological leadership (i.e., not only in the field of BCI technology, but overall) and would this impact be distinctly different if controls were placed primarily on “software” as opposed to hardware, or vice versa?

(7)  How is the future development of artificial intelligence (AI) technology or other emerging technologies likely to impact the development of BCI technology, or vice versa?

(8)  What types of ethical or policy issues are likely to arise from the use of BCI technology (e.g., for medical or military purposes)?

(9)  What kinds of risks and benefits currently exist, or are likely to arise, as a result of the application of BCI technology?

(10)  What are the potential advantages or disadvantages of using invasive and noninvasive BCI chips/sensors and related “software” (e.g., algorithms for signal processing) for specific applications? To what extent would these advantages or disadvantages correspond (or differ) based upon whether invasive or non-invasive BCI chips/sensors and related “software” were being used?

(11)  Are there any BCI technologies that are significantly more vulnerable than others to cybersecurity threats (e.g., military systems employing BCI technologies that could adversely impact U.S. biodefense)?

(12)  What is the potential for transmitted BCI data to be hacked or manipulated to influence the user or machine? Is such data inherently more vulnerable to hacking or manipulation than other forms of data? Would the invasive or non-invasive characteristics of BCI data have any impact on the potential vulnerability of such data?

New Genetic Sequencing Software Controls.

On October 5, 2021, BIS published new narrowly drawn export controls on certain genetic sequencing software. These new export controls, like the BCI Notice discussed above, also were published as part of BIS’s review of “emerging technologies” under the ECRA.  However, unlike the proposed controls under the BCI Notice, the new controls on genetic sequencing software already are in effect (as of October 5, 2021).

The BIS export controls on genetic sequencing software build on existing controls that cover genetic sequencing assemblers and synthesizers that are automated and can generate continuous nucleic acids greater than 1.5 kilobases in length with error rates less than 5% in a single run. Such automated assemblers and synthesizers are controlled under Export Control Classification Number (“ECCN”) 2B352.j. In its new export controls, BIS will control software designed for the automated assemblers and synthesizers in ECCN 2B352.j if such software is capable of designing and building functional genetic elements from digital sequence data the new ECCN 2D352.  In addition, technology for the development of such ECCN 2D352 software will now become subject to the existing controls under ECCN 2E001.

The new controls implemented by ECCNs 2D352 and 2E001 are designed to prevent the export of software and related technology that can be used to generate certain pathogens and toxins without the need to acquire controlled genetic elements and organisms themselves.  BIS noted in issuing these new controls that instructions for creating harmful pathogens and toxins could, accordingly, be manufactured by using 2D352 software, thereby escaping any current export controls that only cover the synthesizers and assemblers as hardware items.

BIS wanted to extend current export controls to cover any such software that is subject to the jurisdiction of BIS under the EAR.  As of October 5, 2021, export licenses are required to export genetic sequencing software controlled under ECCN 2D352 to countries indicated under the Country Chart in Supplement No. 1 of EAR Part 738 and its chemical and biological weapons column two or “CB2” controls. The CB2 controls apply to numerous countries such as China and Russia.

New Intrusion Software Export Controls.

Finally, and separately, BIS published new controls covering intrusion software designed for malicious cyber activities and network surveillance.  BIS is still accepting public comments on the rule until December 6, 2021, although the controls will become effective on January 19, 2022.  BIS is adding three new ECCNs – 4A005, 4D004, and 4E001.c – to control malicious software and related hardware and technology.  All of the new controls target “intrusion software,” defined as software designed to “avoid detection by monitoring tools, or to defeat protective countermeasures, of a computer or network-capable device,” and that can: (a) extract of data or information from a computer or network-capable device, or modify a system or user data; or (b) modify the standard execution path of a program or process in order to allow the execution of externally provided instructions.  However, the term intrusion software does not include any of the following: Hypervisors, debuggers or Software Reverse Engineering (SRE) tools; Digital Rights Management (DRM) software; or Software designed to be installed by manufacturers, administrators or users for the purposes of asset tracking or recovery.

At the same time, BIS also published a new license exception, Authorized Cybersecurity Exports (“ACE”), to permit limited exports of intrusion software.  BIS explained that the new ACE license exception is “necessary to avoid impeding legitimate cybersecurity research and incident response activities.”  ACE allows exports to most destinations, except to destinations embargoed under U.S. law, or to government end-users of certain countries, such as Russia.  ACE is intended to address concerns of the private sector that the new export controls on intrusion software could also reach items intended merely to test cybersecurity defenses or to remedy detected security breaches.

BIS had originally proposed new controls on certain intrusion software in 2015, which resulted in more than 300 comments from industry.  Most of those comments opposed the proposed controls as overly broad, potentially burdensome, and sweeping in numerous common software programs and anti-intrusion software that were not the intended targets of the controls.  As a result of such strong industry opposition, BIS significantly scaled back these new intrusion software controls to those described above and also added the new ACE license exception.

Dorsey’s attorneys can assist companies with assessing the potential impact of the export controls discussed above. For additional information, please feel free to contact the attorneys listed, or see Dorsey’s website at www.dorsey.com.

 

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Minnesota Consumer-Fraud Enforcement: Disclaimers Won’t Cure Deception, and Penalties Can Add Up

Misleading advertising claims can lead to costly consequences. In State of Minnesota ex rel. Ellison v. Wall & Associates, Inc., No. A25-2064, 2026 WL 3118291 (Minn. App. Oct. 19, 2026), the Minnesota Court of Appeals recently affirmed a bench trial verdict against a tax-relief company and two executives for violations of the Minnesota Consumer Fraud Act (“MCFA”) and the Minnesota Deceptive Trade Practices Act (“MDTPA”). The decision, which affirmed a substantial restitution and civil penalty judgment, underscores the broad power of the Minnesota Attorney General to act against deceptive sales practices. The decision also offers practical lessons for businesses seeking to reduce liability risks in consumer-facing communications. Background Wall & Associates (“W&A”), a Virginia-based tax-relief company, marketed assistance to taxpayers seeking relief from outstanding federal and state tax liabilities, often with offers in compromise—agreements to settle tax liabilities for less than the amount owed. 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Contractual Disclaimers Are Not an Automatic Defense to a Misleading Pitch W&A next argued that disclaimers in its client contracts prevented consumers from claiming they had been misled by its advertising. Reiterating that individual reliance is not required under the MCFA and MDTPA, the Court of Appeals held that a contractual disclaimer does not necessarily defeat a claim based on a conflicting oral representation. And on the facts of this case, the Court of Appeals agreed with the district court that W&A’s contractual disclaimers were insufficient given the extensive misrepresentations by W&A and the unequal bargaining power between it and its customers. This holding confirms that contractual disclaimers are not a cure-all for misleading advertising or sales practices. Businesses should review the entire customer journey, including pre-contract representations, as those representations may survive a contractual disclaimer to the contrary. And if faced with litigation, businesses should build a strong record, both at trial and on appeal, showing why any disclaimer is effective in context. The State Has Broad Authority to Seek Restitution W&A also challenged Attorney General Ellison’s authority to seek restitution under the state’s parens patriae authority to protect residents’ collective interests, arguing that injury to only 228 Minnesotans did not affect a sufficiently substantial segment of the population. 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Corporate Counsel Symposium 2026 Materials Hub

Materials Symposium Agenda Sessions 8:30 am - 9:30 am CT Session A: The Corporate Compass: Finding True North When Ethical Duties Conflict Philip Kaplan, Senior Legal Counsel, Howden Re Lucia Suljic, Vice President, Corporate Legal, Canon USA Nicole Stanton, Partner & Deputy General Counsel, Dorsey & Whitney LLP This panel addresses ethical obligations of in-house counsel, including balancing obligations and duties that may conflict with each other. How should a responsible in-house lawyer deal with those challenging situations? Rather than stick to an academic discussion, this panel will revolve around a series of practical scenarios that are designed to be realistic and timely, including situations where counsel is asked to represent both the company and an individual, how and when to disclose uncomfortable facts and inconvenient documents, issues involving changing firms and companies, and multijurisdictional practice. 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Observations on the SEC’s 2027 Examination Priorities

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Reviewing disclosures on allocations, leverage, and affiliated service providers. The 2027 Exam Priorities identify disclosures related to certain investments and allocations, the use of debt and fund-level lines of credit, and the use of affiliated service providers as examples. Confirming the accuracy of fee and expense calculations. The Division states that it will assess the accuracy of fee and expense calculations at both the fund and investment levels, and it identifies fee rebates, cash management, quid pro quo arrangements, deposits, and withdrawals as areas in which economic conflicts of interest may affect the impartiality of advice. Reviewing recommendations of illiquid or hard-to-trade products. The Division states that it will prioritize advisers that recommend products that are difficult to trade, have unusual features, or are illiquid, including loans provided by private funds or BDCs and investments in private companies through SPVs. Confirming that the compliance program is implemented and reviewed. The Division states that it will review compliance program components such as marketing, valuation, and custody, as appropriate, and will typically analyze the annual compliance review. It will also focus on compliance practices when advisers have started advising new asset classes or clients or grown through mergers or acquisitions. 1 SEC Division of Examinations 2027 Examination Priorities. 2 See Dorsey’s Client Alert on the SEC’s fiscal year 2026 exam priorities.