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Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on Health Chair Brett Guthrie (R-KY), and Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA), on behalf of the Health and Oversight Subcommittee Republicans, today sent a letter to Department of Health and Human Services (HHS) Inspector General (IG) Christi Grimm. The letter highlights concerns surrounding improper Medicaid payments and challenges States face in maintaining accurate enrollment during and after the eligibility redetermination process.  “It is critical that CMS and States take action to reduce the number of improper Medicaid payments to ensure that taxpayer dollars are spent to care for the most vulnerable who Medicaid was designed to help,” Chairs Rodgers, Guthrie, and Griffith wrote.   Background :  In response to the COVID-19 pandemic, Congress passed the Families First Coronavirus Response Act (FFCRA), which included provisions for enhanced Federal Medical Assistance Percentage (FMAP) of 6.2% for States and required continuous Medicaid coverage through the COVID-19 Public Health Emergency (PHE).  The PHE led to a surge in Medicaid enrollment, increasing from 70 million to nearly 95 million individuals.  As part of the 2023 Consolidated Appropriations Act, States are authorized to start the process of redetermining Medicaid eligibility from April 1, 2023.  Research demonstrates that even before the COVID-19 pandemic, maintaining accurate Medicaid enrollment posed a significant challenge for CMS.  Past audits from the HHS IG have found inaccuracies in Medicaid enrollment resulted in improper payments.  The Chairs requested a briefing from the Office of the Inspector General as well as an audit that reviews and analyzes the following information regarding ineligible beneficiaries:  The reason for beneficiaries’ ineligibility  The types of factors and information considered at the time of enrollment  The causes of incorrect eligibility determinations  The approximate time individuals were ineligibly enrolled  The approximate dollar amount spent on recipients who were ineligible  The approximate dollar amount delivered to insurance companies on behalf of ineligible enrollees  CLICK HERE to read the letter to HHS IG Grimm. 

Did NIH Know that Decorated Scientist Planned to Conduct Gain-of-Function Research?  Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on Health Chair Brett Guthrie (R-KY), and Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA), on behalf of the Health and Oversight subcommittee Republicans, sent a letter to the Department of Health and Human Services requesting that the National Institutes of Health’s (NIH) top expert on pox viruses sit for a videotaped, transcribed interview regarding the mysterious discontinuation of his proposed experiment to supercharge the mpox virus.  BACKGROUND:   In a September 2022 Science article , Dr. Bernard Moss of the National Institute of Allergy and Infectious Diseases (NIAID) discussed a specific mpox project:  From the article: “Moss has been trying for years to figure out the crucial difference between two variants of monkeypox virus: clade 2, which until recently was found only in West Africa and is now causing the global outbreak, and clade 1, believed to be much deadlier, which has caused outbreaks in the Democratic Republic of Congo for many decades. He’s found that clade 1 virus can kill a mouse at levels 1000 times lower than those needed with clade 2. To find out why, Moss and his colleagues swapped dozens of clade 2 genes, one at a time, into clade 1 virus, hoping to see it become less deadly, but with no luck so far. Now, they are planning to try the opposite, endowing clade 2 virus with genes from its deadlier relative.”  The effect of the project would be to supercharge the less lethal but much more transmissible variant of the mpox virus that caused the recent U.S. epidemic by combining it with a highly lethal variant found only in the Congo Basin.  Energy and Commerce Republicans requested in a March 30, 2023, letter documents related to the experiment described in the Science article.  On April 26, 2023, NIH responded by noting the proposal did not go forward but did not explain how that occurred or how NIH could even be sure that the experiment was not already conducted.  KEY EXCERPT:   “You informed us that the study discussed by Dr. Moss 'has not been formally proposed, and NIAID has no plans to move forward with this research.' This is a stunning admission. Dr. Moss has been with the NIH since 1966, is one of the leading authorities on pox viruses, and one of the NIH’s most accomplished researchers. He has received numerous awards and prizes. He was elected to the National Academy of Sciences, American Academy of Microbiology, Fellow of the American Association for the Advancement of Science, and president of the American Society for Virology. Dr. Moss is currently an editor of Virology and a member of several editorial boards. Dr. Moss’s comments to Science indicate to us that he gave the study in question much thought and effort, and that he believed in going forward with the mpox study. The admission that he did not formally propose this research, and the NIAID has no plans to pursue it seems extraordinary. It seems unlikely that Dr. Moss changed his mind. On the other hand, it is hard to believe the NIAID has apparently overruled one of its most highly respected scientists. These circumstances demand a detailed explanation about what happened with this research project publicized by Dr. Moss.”  CLICK HERE to read the full letter. 

Lawmakers leave door open to compelling testimony if Becerra refuses to cooperate House Republicans are holding the Biden administration accountable for the surge of migrants flowing across our border illegally and the exploitation of unaccompanied migrant children that has followed.  Despite publicly committing to Subcommittee on Oversight and Investigations Chair Morgan Griffith that he would “absolutely” be willing to appear before the Subcommittee, Health and Human Services (HHS) Secretary Xavier Becerra has failed to make good on his promise.  On Friday, E&C Chair Cathy McMorris Rodgers and Subcommittee Chair Griffith sent Secretary Becerra a letter demanding that he testify. In the letter , the Chairs outlined the great lengths to which they’ve gone to accommodate Secretary Becerra’s travel schedule and venue preference. They have offered a hearing date of June 13 or June 14.  READ: Exclusive Coverage on FOX News : Becerra’s appearance is being sought as the U.S. is continuing to deal with a migrant crisis at the southern border now in its third year. While the primary agency dealing with the migrant surge is the Department of Homeland Security, unaccompanied minors encountered by  Border Patrol  are transferred into HHS custody, at which point officials attempt to find sponsors—typically a relative or parent—for them.  According to Customs and Border Protection (CBP) statistics, the number of unaccompanied alien children (UACs) who arrive at the border has increased from 33,239 in fiscal year 2020 to more than 146,000 in fiscal year 2021 and 152,000 in fiscal year 2022. So far in fiscal year 2023, there have been more than 70,000 encounters of UACs.  […]  The Times reported how officials  reportedly ignored  signs of "explosive" growth in the child labor force, while staff members claimed Becerra pushed for discharging minors even quicker.  "If Henry Ford had seen this in his plants, he would never have become rich and famous," he was quoted by the Times as telling staff. "This is not the way you do an assembly line."  […]  "In the event you do not select either of the above dates, the Committee will be forced to consider other avenues to secure testimony from you that is needed to fulfill our constitutional mandate to oversee the administration of these programs," they say.   CLICK HERE to read more from FOX News.  CLICK HERE to read the full letter to Secretary Becerra. 

Report alleges patients frequently forced to pay out-of-pocket for services that should be covered Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on Health Chair Brett Guthrie (R-KY), and Subcommittee on Oversight and Investigations Chair Morgan Griffith (VA), on behalf of the Health and Oversight Subcommittee Republicans, wrote to the President and CEO of The Cigna Group regarding an investigative report by ProPublica.   In the letter, the members note that Cigna disputes the report as “biased” and “incomplete,” and they ask the insurance company to respond to the allegations that it uses automation and AI technology to deny claims.   According to the report titled “How Cigna Saves Millions by Having its Doctors Reject Claims Without Reading Them,” which focuses on Cigna’s procedure-to-diagnosis (PXDX) review process:   The PXDX review process denies payments for claims indiscriminately, potentially leading to improper denials of coverage for medically necessary tests and procedures.   The process automatically categorizes certain claims as “unnecessary” using an algorithm in place of a clinician’s judgement.   Patients are then reportedly told that a clinician has decided such claims were not necessary and therefore not covered, despite the clinician having never reviewed individual claims.   Only an estimated five percent of policy-holders appeal denials of coverage.   By contrast, nearly one-in-five prior authorization denials in Cigna’s Medicare Advantage plans were appealed.   Why It Matters:    80 percent of Medicare Advantage coverage denials were overturned, suggesting that Cigna’s PXDX review process is leading to patients paying out-of-pocket for medical care that should be covered under their insurance policy contract.   The Chairs requested Cigna turn over documents related to the PXDX process and answer the following questions by May 30, 2023:   Describe in detail the PXDX review process, including its development, implementation, and ongoing usage.   Identify all insurance plans offered or administered by Cigna whose claims are subject to PXDX review, including, if applicable, Medicare Advantage plans.   Identify all medical directors employed by Cigna who review, submit, or approve coverage denials generated by the PXDX review process, include in your response the medical directors’ work email address, the nature of claims reviewed, and tenure at the company.   Provide the following statistics for plan year 2022 for both commercial and government contracts (broken down by government program):   The number of claims reviewed by the PXDX process;   The number of claims denied under the PXDX process;   The number of claims reviewed and denied by each clinician employed by Cigna who participates in the claim review process;   The number of claims denied by each clinician employed by Cigna and the number of claims that were actually reviewed by such clinicians;   The number of claims denied under the PXDX process that were appealed; and   The number of claims denied under the PXDX process that were appealed and overturned.   In addition, the letter serves as a request to preserve all existing and future documents related to the PXDX process.   CLICK HERE to read the full letter. 

Washington, D.C. —  Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA) delivered the following opening remarks during today’s Oversight and Investigations Subcommittee hearing titled “ Examining the Root Causes of Drug Shortages: Challenges in Pharmaceutical Drug Supply Chains .” Excerpts and highlights below: THE SCALE OF THE PRESCRIPTION DRUG SHORTAGE “This morning’s hearing will examine the very serious and growing problem of prescription drug shortages. “Americans need more reliable access to life saving drugs. “According to the American Society of Health System Pharmacists we currently have over 247 active drug shortages. “Between 2021 and 2022 drug shortages increased by almost 30%. “It is unbelievable that in our great country there is a shortage of drugs to treat childhood cancer and that is just one example. “It's even more galling when you consider that most shortages are in the generic drug space where there should be competition. “The median price of a drug in shortage between 2013 and 2017 was less than 9 dollars per treatment dose. “Generic drugs account for 90% of all prescriptions, but only 17% of drug spending. “Generics are perhaps the only significant segment of our healthcare industry where costs haven’t increased faster than inflation.” ROOT CAUSES OF SHORTAGES “The generic pharmaceutical industry is plagued with a myriad of issues leading to drug shortages. “We have an economic environment so unappealing to manufacturers that life-saving drugs are produced by one, or at most, two companies worldwide, often at an unsustainable, artificially low price. “There is a broad consensus that the root cause of drug shortages is a profound market failure caused by economic forces unique to the drug market. “Middlemen such as Pharmaceutical Benefit Managers or Group Purchasing Organizations do not care to look for ways to mitigate shortages. “By one count, for every 100 dollars spent on a generic prescription drug 44 dollars go to a middleman. “The three largest Pharmaceutical Benefit Managers control around 80% of the commercial drug sales. “The four largest Group Purchasing Organizations control 90 percent of the medical supply market and have massive market power. “They could help end drug shortages by prioritizing generic drugs availability and quality. “Instead, they use their market power to force ‘race to the bottom pricing’ without consideration for quality or availability. “Their contracts with generic drug manufacturers consist of a ‘take it or leave it’ approach. “Leaving the generic manufacturer, the option to either comply or lose access.” OUR SHRINKING MANUFACTURING CAPABILITY “Over the past 10 years, the United States has seen dozens of generic drug manufacturing facilities close. And this shortage problem isn’t limited to just closings. “The typical generic drug has just two manufacturing facilities. “We currently do not fully utilize the factories we have. As Professor Sardella’s notes, we only use about half of our current generic manufacturing capacity. “We now have fewer manufacturing facilities both in the U.S. and globally and our supply chain has proven to be fragile and vulnerable to disruption. “Forty percent of generic drugs are made at just a single facility. Thus, even the temporary shutdown of a single facility triggers a shortage. “We are also far too dependent on foreign countries for generic drugs and active pharmaceutical ingredients, or API, especially China and India. “Our dependence on China represents a serious national security risk. “China’s new interpretation of its national security law may make FDA’s already anemic inspection program in that country a crime.” THE FDA’S FAILURES “As we are holding this hearing, FDA Commissioner Califf is appearing before our Health Subcommittee. “All too often his agency has made drug shortages worse and left us more vulnerable. “The FDA’s response to shortages is to allow for foreign made generics and API to come unfettered to the US market. “The FDA claims to be focused on collecting information, but it does not effectively use the information it already has. “We need an FDA that prioritizes applications from U.S. manufacturers and gives companies the flexibly to address shortages with resources based here. “Solving drugs shortages is going to require an all-of-the-above approach. “Purchasers of generic drugs must incentivize quality and reliability in generic drugs. And we must always keep in mind the human toll of drug shortages. “I look forward to hearing from our witnesses today who are all working in innovative ways to help solve drug shortages.”

Members press companies to answer what information is collected and where it is sold Washington, D.C. — House Energy and Commerce Committee Republicans, led by Chair Cathy McMorris Rodgers (R-WA) and Committee Democrats, led by Ranking Member Frank Pallone, Jr. (D-NJ), today wrote to the heads of data broker companies, requesting information to help the Committee protect Americans’ data from misuse. They were joined by Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA) and Ranking Member Kathy Castor (D-FL), Subcommittee on Innovation, Data and Commerce Chair Gus Bilirakis (R-FL) and Ranking Member Jan Schakowsky (D-IL), Subcommittee on Health Chair Brett Guthrie (R-KY) and Ranking Member Anna G. Eshoo (D-CA), and Subcommittee on Communications and Technology Chair Bob Latta (R-OH) and Ranking Member Doris Matsui (D-CA).  BACKGROUND:   The Subcommittee on Oversight and Investigations launched a bipartisan investigation at a hearing on April 19, 2023, titled “Who is Selling Your Data: A Critical Examination of the Role of Data Brokers in the Digital Economy.”  Data brokers purchase, collect, aggregate, license, sell, or otherwise share a wide range of information from Americans, including but not limited to demographic, location, and health data.  These companies profit from trading in Americans’ personal information, including sensitive information, often with little government oversight and in some cases, without any concern for how buyers use the consumer data that they purchase from brokers.  A recent study from Duke University found, for example, that “some data brokers are marketing highly sensitive data on individuals’ mental health conditions on the open market, with seemingly minimal vetting of customers and seemingly few controls on the use of purchased data.”  KEY EXCERPT:   “American privacy concerns in the data broker industry are not new, and existing laws do not sufficiently protect Americans’ data from misuse. In 2014, the FTC issued a report recommending that Congress require data brokers to increase transparency and give Americans more control of their data. However, data brokers can easily circumvent existing rules and laws regarding the collection and sharing of certain types of data, such as HIPAA.   “Enacting a comprehensive federal privacy law is a top priority for the Committee on Energy and Commerce. Currently, Americans do not have control over whether and where their personal data is sold and shared; they have no guaranteed way to access, delete, or correct their data; and, they have no ability to stop the unchecked collection of their sensitive personal information. According to the Electronic Privacy Information Center, the overcollection and secondary uses of personal data, including the sale to and use by data brokers, are inconsistent with the reasonable expectations of online consumers and may lead to discriminatory targeting that violates the privacy and autonomy of consumers.”  The leaders asked the companies for information pertinent to helping the Committee understand how data brokers purchase, collect, use, license, and sell Americans’ data, including:  What data elements do you possess on Americans and market to your clients?   In particular, do you possess any of the following:  Americans’ health data? If yes, what kind of health data?  Americans’ location data? If yes, what data elements?  Americans’ phone data, such as data on any apps downloaded on their mobile devices? If yes, what data elements?  Information revealing Americans’ purchase history? If yes, what data elements?  Information about children under the age of 13?  Information about children between the ages of 13 and 18?  Are there any categories of Americans’ personal information that you will not purchase, collect, aggregate, license, or sell and, if so, what categories are those?  When you license, sell, or otherwise share Americans’ personal information with your clients, do you require your clients to disclose the purpose(s) for which they will use the data?   If so, what do you do, if anything, to confirm they are using the data for the stated purpose(s)?  How much money did you spend in each of the past five years on purchasing or licensing Americans’ personal information?  What percentage of your annual revenue for each of the past five years was derived from selling or licensing Americans’ personal information?  How many clients did you sell or license Americans’ personal information to?  Does your company use the personal information of Americans that you purchase, collect, or aggregate to categorize people based on income, sex, age, race, or other categories?  What steps, if any, does your company take to protect data of users under eighteen?  When you become aware that you or your clients have transferred Americans’ personal information to a foreign adversary or a company beholden to a foreign adversary—currently defined by the Secretary of Commerce to include China, Russia, North Korea, Cuba, the Maduro regime in Venezuela, and Iran—do you notify the individual(s) whose personal information has been transferred or any U.S. government entity? If not, why not?  You can view the letters below:  Acxiom LLC AtData Babel Street   CoreLogic Solutions, LLC   Epsilon Data Management, LLC Equifax   Experian   Gravy Analytics, Inc. Intelius, LLC Kochava Inc. LiveRamp, Inc. Mylife   Oracle America, Inc.   PeopleConnect, Inc. Placer.ai   RELX Safegraph Inc. Spokeo, Inc.   Thomson Reuters   TransUnion   Verisk Analytics   Whitepages, Inc.

Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on Health Chair Brett Guthrie (R-VA), and Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA) issued the following statements after the National Institutes of Health (NIH) restored its grant to EcoHealth Alliance (EHA) that was previously suspended.  Chair Rodgers : “It’s beyond outrageous that NIH would restore funding to this taxpayer funded grant despite well-documented, egregious failures by EcoHealth to comply with grant requirements and NIH’s failure to conduct proper oversight of the grant. The Department of Health and Human Services and the NIH must explain to the American people why it would take this controversial and irresponsible action.”  Health Subcommittee Chair Guthrie : “EcoHealth Alliance not only has documented negligence, ignorance, and failures in following the rules of a taxpayer-funded grant, but also is the subject of a congressional investigation on its research with the Wuhan Institute of Virology. It is shocking and disappointing that the NIH is restoring a taxpayer-funded grant to EcoHealth Alliance. We’re going to get answers on behalf of the American people why their money is being awarded to EcoHealth Alliance.”  Oversight Subcommittee Chair Griffith : “It’s absolutely reckless that the NIH has renewed a grant for EcoHealth Alliance given their negligence and the breach of their contract with the NIH on the coronavirus research done at the Wuhan Institute of Virology. It is now believed likely that COVID-19 was the result of a lab incident at the Wuhan Institute.  “From my observations, EcoHealth Alliance has not been contrite about their failures. And even worse, they have refused to cooperate with Congress in our attempts to get information about the research they were doing at the Wuhan Institute.  “Until they can demonstrate a willingness to work with Congress to resolve outstanding questions and fulfill all of the terms of their federal contracts, paid for with American taxpayer dollars, all funding should remain suspended, and no new contracts should be awarded.”  In response to the announcement and previous testimony before Congress, Chair Rodgers, Guthrie, and Griffith, on behalf of the Health and Oversight Subcommittee Republicans, sent a letter to Department of Health and Human Services Inspector General Christi Grimm (HHS IG), asking for her office’s audit file which supported the decision not to recommend baring EHA from receiving NIH grants. The decision not to refer EHA for debarment, despite an HHS IG report detailing NIH’s failures to oversee the grant to EHA, is under investigation by the Committee.  You can read that letter here .  Additional Background:  January 2023 HHS OIG Report: The National Institutes of Health and EcoHealth Alliance Did Not Effectively Monitor Awards and Subawards, Resulting in Missed Opportunities to Oversee Research and Other Deficiencies  The HHS IG’S Key Findings:  “Despite identifying potential risks associated with research being performed under the EcoHealth awards, we found that NIH did not effectively monitor or take timely action to address EcoHealth's compliance with some requirements.”  “Although NIH and EcoHealth had established monitoring procedures, we found deficiencies in complying with those procedures limited NIH and EcoHealth's ability to effectively monitor Federal grant awards and subawards to understand the nature of the research conducted, identify potential problem areas, and take corrective action.”  Read the full report here .  Chair Rodgers: HHS’s OIG Report Confirms our Concerns with NIH’s Funding of EcoHealth Alliance  Key Quote: “The American people have a right to know what types of potentially risky research their tax dollars are funding. This OIG Report reaffirms many issues Energy and Commerce Republicans have continued to raise with NIH’s negligence in holding EcoHealth Alliance accountable to the terms of grant agreements. Furthermore, the report raises even more questions from the Committee about the apparent special treatment given to EcoHealth Alliance.”  Read more here .  October 2022 E&C Republicans to NIH: Why Resume Taxpayer-Supported Grant Funding to EcoHealth?  Key Quote: “The NIH has a responsibility to the American people to ensure research supported by taxpayer dollars is conducted with the highest standard of integrity, transparency, and safety. To that end, agency officials must answer why they are considering restoring funding to EcoHealth Alliance,” said Chairs Rodgers, Guthrie, and Griffith.  Read the full letter here . 

CDC Must Provide Information from Internal Audit Before Requesting More Authority from Congress Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on Health Chair Brett Guthrie (R-KY), and Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA) today sent a letter to Centers for Disease Control and Prevention (CDC) Director Rochelle Walensky, requesting information related to its efforts to its Moving Forward Initiative . The letter, sent on behalf of the Republican members of the subcommittees, also serves as a notice to preserve all documents and communications regarding the effort.  KEY EXCERPTS:   “As you have publicly acknowledged, the CDC’s response to the COVID-19 pandemic response has been widely criticized. From early pandemic test kit failures to the revelation that teachers’ unions were provided an opportunity to opine on and revise the CDC’s school reopening guidance, the CDC committed multiple unforced errors during the COVID-19 response. More recently, the CDC’s insistence that children as young as three years old continue to receive COVID-19 shots and wear masks has made it an outlier among global public health agencies. In short, CDC has lost the American people’s trust. ”  […]  “ The CDC must provide the Committee with more than a cursory, summarized overview of the findings of the Moving Forward Initiative before the Committee can even begin to consider the agency’s request for additional authority. According to principles for government reorganization recommended by the Government Accountability Office (GAO), Congress ‘has an important role to play in both its legislative and oversight capacities in establishing, monitoring, and maintaining both governmentwide and agency-specific management reforms.’ This Committee has serious reservations regarding CDC’s approach to public engagement, stakeholder outreach, and information gathering during the Moving Forward Initiative . The CDC has been rightly criticized in the past for its insular culture and lack of transparency. To restore public trust and implement effective reforms, the agency must be more forthcoming to this Committee, Congress, and the American people.”  KEY FACTS AND BACKGROUND:   Timeline : The CDC is currently implementing its Moving Forward Initiative , which it started in April 2022 but did not publicly announce until August 2022.  Structure : The Moving Forward Initiative appears to consist of two parallel reviews with a resulting reorganization of the agency based on the reviews’ findings.   The first review, titled the Scientific and Programmatic Review , focused on identifying methods “to improve and institutionalize how CDC develops and deploys its science, both in pandemic and non-emergency times.”   The second, titled the Structural Review , sought to “gather feedback on the agency’s current processes, systems, and structure and solicit suggestions for strategic change, with a strong focus on the agency’s core capabilities.”  Lack of Transparency : The CDC conducted the Moving Forward Initiative largely in secret.   The public notice and comment period was only open for 10 days and resulted in just three submitted public comments.  The CDC appears to have only held one public meeting at which the initiative was discussed.  In contrast with the small amount of public input allowed by the CDC, the Scientific and Programmatic Review included approximately 120 interviews with internal CDC leadership, staff, and unidentified external partners presumably solicited by the CDC for input.  Similarly, the Structural Review included more than 50 internal interviews.  None of the interviews conducted during the reorganization have been made public, nor has the CDC publicly revealed the outside stakeholders it consulted during the Moving Forward Initiative .   To date, the CDC has made public only two short summaries of the reviews’ findings.  Taken together, those summaries total eight pages.   Resulting Action : CDC is undertaking a large-scale reorganization.  The Federal Register notice announcing the reorganization—one of the few public documents outlining any details on the effort—states the reorganization eliminated 20 different offices, divisions, and centers while creating 16 new entities within the agency.  Most notably, the reorganization appears to expand greatly the size and power of the Office of the Director at the expense of the agency’s national centers.  Request for Additional Authority : Beyond structural changes, the CDC is using its findings of the Moving Forward Initiative to justify its request to Congress for additional authority to, among other things, mandate data reporting from state, local, territorial, and tribal (SLTT) public health agencies.  This authority would dramatically change the nature of CDC’s relationship with its SLTT partners from one based on the principles of cooperative federalism to one where CDC can compel SLTT agencies to hand over individualized public health data.   To date, CDC has not articulated any restrictions on how it would exercise the requested data authority.   CDC’s past data collection practices suggest the agency would use such authority on matters totally outside of CDC’s core mission.  CLICK HERE to read the letter. 

Committee seeks to improve pandemic preparedness, strengthen grant oversight, and enhance the biosafety of lab and field research  Washington, D.C. — House Energy and Commerce Committee Chair Cathy McMorris Rodgers (R-WA), Subcommittee on O versight and Investigations Chair Morgan Griffith (R-VA), and Subcommittee on Health Chair Brett Guthrie (R-KY) today on behalf of the Oversight and Health subcommittee Republican members wrote to Dr. Lawrence Tabak, the senior official who is performing the duties of Director of the Natio nal Institutes of Health (NIH). They requested information to bolster the committee’s ongoing investigation into the origins of COVID-19 regarding any early sequences, data from early cases, or other pertinent documents related to the early phase of the pandemic. The letter follows New York Times April 23, 2023, reporting that the Chinese Communist Party forced a team of scientists from the United States and China to withdraw an early study on COVID-19:  Early in 2020, on the same day that a frightening new illness officially got the name Covid-19, a team of scientists from the United States and China released critical data showing how quickly the virus was spreading, and who was dying.   The study was cited in health warnings around the world and appeared to be a model of international collaboration in a moment of crisis.   Within days, though, the researchers quietly withdrew the paper, which was replaced online by a message telling scientists not to cite it. A few observers took note of the peculiar move, but the whole episode quickly faded amid the frenzy of the coronavirus pandemic.   What is now clear is that the study was not removed because of faulty research. Instead, it was withdrawn at the direction of Chinese health officials amid a crackdown on science. The Chairs’ letter, which serves as a formal notice to preserve all relevant documents and records, requests the following unredacted information by May 17, 2023:  All correspondence between Lili Ren and the National Center for Biotechnology Information (NCBI) or Genbank in the timeframe from January 1, 2019, to March 15, 2020, as well as any associated data files.  All documents, including the research proposal and progress reports, related to NIH grant R01AI098775.  All documents, including the research proposal and progress reports, related to NIH grant R01AI139092.  The unredacted version of the Freedom of Information Act (FOIA) disclosure found here .   The unredacted version of the FOIA disclosure found  here . CLICK HERE to read the full letter to Dr. Tabak.