Hassan, Murray, Colleagues’ Request Follows Revelations that McKinsey Consulted for FDA on Opioid-Related Projects While Working for Opioid Manufacturers Like Purdue Pharma
(Washington, D.C.) – U.S. Senator Patty Murray (D-WA), Chair of the Senate Health, Education, Labor, and Pensions (HELP) Committee, joined a group of her colleagues led by Senator Maggie Hassan (D-NH) in calling for an investigation into the failure of the consulting firm McKinsey & Company to disclose potential conflicts of interest when the company was simultaneously working with the Food and Drug Administration (FDA) on issues related to opioids and for numerous opioid companies, including Purdue Pharma. As the opioid crisis continues to devastate communities, the Senators are calling for a Health and Human Services Inspector General investigation into the FDA’s work with McKinsey and the FDA’s conflict-of-interest disclosure policies for contractors to ensure transparency.
The letter was led by Senator Maggie Hassan (D-NH), Chair of the Emerging Threats and Spending Oversight Subcommittee, and was also signed by Senators Tammy Baldwin (D-WI), Joe Manchin (D-WV), Ed Markey (D-MA), Elizabeth Warren (D-MA), and Sheldon Whitehouse (D-RI).
“While working for clients involved in manufacturing, distributing, and selling opioids, McKinsey simultaneously worked on projects for FDA, including projects for the FDA center responsible for approving new drugs, like opioids. Government contracting databases show that since 2008, McKinsey has been hired by FDA on numerous occasions, earning more than $140 million,” the Senators wrote to Christi A. Grimm, Inspector General for the Department of Health and Human Services.
Following previous bipartisan efforts to push for answers from the FDA after learning from media reports that McKinsey did not reveal potential conflicts of interest to the FDA while they were contracted to work for the agency, the FDA responded that it had not known about McKinsey’s work with Purdue Pharma until media reports surfaced in 2021.
In their letter, the Senators continued, “Despite these reports, FDA did not conduct any additional contract reviews or discuss with McKinsey conflicts of interest and the firm’s failure to disclose them in earlier contract applications. Furthermore, it is unclear whether FDA has altered or improved its processes and procedures to prevent similar nondisclosures of conflicts of interest in future contracts.”
The Senators are calling on the Inspector General to review the actions of McKinsey and FDA as it pertains to these conflicts of interests and McKinsey’s failures to disclose them, and what actions the agency should take to help ensure that these failures don’t occur in the future.
To read the full letter, click here or see below.
Dear Inspector General Grimm:
We are writing to request that the Office of Inspector General for the Department of Health and Human Services open an investigation into the failure of consulting firm McKinsey & Company (“McKinsey”) to disclose potential conflicts of interest when McKinsey entered into contracts with the Food and Drug Administration (“FDA”) on issues related to opioids while simultaneously working for numerous opioid companies. We also write to request that your office review FDA’s contracting policies and procedures and determine how the agency can ensure that future contractors adequately disclose all potential conflicts.
For more than a decade, McKinsey has advised companies throughout the opioid industry. McKinsey recently settled with 49 states Attorneys General for $573 million due to actions that exacerbated the opioid epidemic, including advising Purdue Pharma on how to “turbocharge” sales of OxyContin. Former clients also include opioid manufacturers Johnson & Johnson, Mallinckrodt, and Endo International, as well as major opioid distributors and retailers.
While working for clients involved in manufacturing, distributing, and selling opioids, McKinsey simultaneously worked on projects for FDA, including projects for the FDA center responsible for approving new drugs, like opioids. Government contracting databases show that since 2008, McKinsey has been hired by FDA on numerous occasions, earning more than $140 million. The firm was deeply involved with the Center for Drug Evaluation and Research (CDER), FDA’s principal center for approving new drugs, including opioids: at least 17 of McKinsey’s FDA contracts, totaling more than $48 million, call on the firm to work with CDER. In 2008, McKinsey began working with Purdue on how to develop its FDA-mandated proposed Risk Evaluation and Mitigation Strategies (REMS), a drug safety program overseen by CDER, that required manufacturers to communicate safety risks to patients, pharmacists, and other health care providers. McKinsey built a strategy for Purdue and other opioid manufacturers to “play, delay, pre-empt, and band together,” by “jointly develop[ing] FDA response strategy,” “shar[ing] abuse mitigation strategies,” and “formulat[ing] arguments to defend against strict treatment by the FDA.” When the finalized REMS for opioid products was announced in 2012, it was largely devoid of the restrictions that FDA had initially proposed.
FDA requires that contractors such as McKinsey agree to its Organizational Conflicts of Interest (OCI) policy, as set out by the Federal Acquisition Regulation. Last August, some of our offices sent a letter to FDA, requesting further information about these conflicts of interest and whether McKinsey disclosed the required OCI to the agency during the contracting process. FDA responded to our letter two months later on October 22, 2021, and stated that “FDA is not aware of any disclosures made by McKinsey vis-a-vis OCI in relation to these orders. FDA cannot speculate on why McKinsey did not consider any actual or apparent OCI to be sufficient to require reporting as directed by the contract requirements.” Despite the conflicts implicit in its simultaneous work for opioid companies and for the FDA, McKinsey apparently never notified the agency of potential OCI. And as FDA stated in its recent letter, the responsibility for identifying conflicts of interest fell entirely on McKinsey: “FDA relies on the contractor to assess and report potential OCI and submit mitigation plans for review.” Despite the requirements in its contracts, McKinsey failed to make any disclosures to FDA with regard to its many conflicts of interest and in fact repeatedly warranted just the opposite – that it had no such conflicts.
In its response, FDA also stated that it only became aware of McKinsey’s past work for opioid industry clients in early 2021, when these ties were widely reported on in the media. However, the first reports on McKinsey’s extensive work for Purdue Pharma surfaced in early 2019. In the interim, McKinsey continued to perform work for FDA; contracting databases show that from February 2019 to January 2021, the firm received more than $20 million in new contracts from the FDA. Despite these reports, FDA did not conduct any additional contract reviews or discuss with McKinsey conflicts of interest and the firm’s failure to disclose them in earlier contract applications. Furthermore, it is unclear whether FDA has altered or improved its processes and procedures to prevent similar nondisclosures of conflicts of interest in future contracts.
The Office of the Inspector General for the United States Department of Health & Human Services is uniquely situated to review the actions of McKinsey and FDA as it pertains to these conflicts of interests and the failures to disclose them. As part of your review, we ask that you specifically address the following issues:
At a time when the opioid epidemic is still raging nationwide, we must hold those who fueled it accountable and take action to prevent similar failures in the future. We thank you for your prompt attention to this matter.