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FDA Postpones DSCSA Provision Enforcement by Three Years

Client Alert | 2 min read | 11.05.20

The U.S. Food and Drug Administration (FDA) has again postponed the enforcement of certain requirements under the Drug Supply Chain Security Act (DSCSA), this time by three years. 

On October 22, 2020, the FDA issued guidance stating that enforcement of wholesale distributor compliance with the DSCSA’s saleable return verification requirement will be postponed until 2023. The FDA guidance states that it “does not intend to take action against wholesale distributors who do not, prior to November 27, 2023, verify the product identifier prior to further distributing returned product as required under the” saleable return verification requirement of the DSCSA. This extension comes just over a year after the FDA’s September 2019 guidance, which initially postponed enforcement of the saleable return verification until November 27, 2020.

The FDA has indicated that multiple entities in the supply chain urged FDA to delay enforcement due to concerns with industry-wide readiness for implementation. “Specifically, comments received point out continuing challenges posed by the large volume of saleable returned product, explaining that wholesale distributors still need more time to test verification systems using real-time volumes of saleable returned product with all trading partners involved, as opposed to using small-scale pilot test projects.”

Relatedly, the FDA’s October 22, 2020 guidance states that, prior to November 27, 2023, the FDA “does not intend to take action against a wholesale distributor for providing a transaction statement to a subsequent purchaser of a product on the basis that such wholesale distributor does not yet have systems and processes in place to comply with the saleable return verification requirements under section 582(c)(4)(D) of the FD&C Act.”

The FDA’s guidance also delays until November 27, 2023, enforcement against dispensers who do not verify the statutorily-designated portion of product identifiers of suspect product, as well as enforcement of dispenser verification of product when responding to a notification of illegitimate product from FDA or another trading partner. 

The FDA expressed its expectation that wholesale distributors and dispensers will use this delay to ensure the necessary systems and processes for compliance with the saleable return verification requirements are in place by November 27, 2023. The additional time provided by this guidance may allow for new technologies and solutions to ensure DSCSA compliance.

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Bid Protests: GAO Reminds Would-Be Protesters – Timing Is Everything

When to file a protest challenging an agency’s corrective action is an issue that has confused protesters for over a decade since GAO’s Domain Name Alliance Registry, B‑310803.2, Aug. 18, 2008, 2008 CPD ¶ 168 decision.  In Domain Name, GAO held where a protester essentially challenges the “ground rules” of corrective action, that protest must be filed pre-award or risk being dismissed as untimely.  This has led to the proliferation of overly cautious protesters bringing pre-award challenges to corrective actions only to have GAO dismiss such protests as merely anticipating improper agency action and therefore premature.  Indeed, the line between a timely and untimely corrective action protest is unclear.  And that confusion persists, as evidenced in two recent GAO dismissals—General Dynamics Information Technology, Inc., B-422421.6, B-422421.7, July 17, 2024, and Peraton Inc., B-422409.2, B‑422409.3, July 22, 2024....