Joshua McCann is committed to working with health care clients to achieve efficient and innovative outcomes for their immediate and long-term goals. He applies his understanding of health care issues towards representing hospitals, pharmacies, physician groups and other health care professionals and organizations in a variety of health care matters.

Joshua is a licensed pharmacist and is member of Polsinelli’s pharmacy and 340B teams and assists with day-to-day regulatory, audit and transactional matters. He received his Pharm.D. from the University of Oklahoma College of Pharmacy. Prior to earning his law degree, Joshua practiced as a pharmacist in a variety of settings. He has extensive experience in pharmacy compounding and the various regulatory and legal issues facing pharmacy clients. Joshua uses his hands-on experience and understanding to advise a broad set of health care entities.

Education

  • University of Tulsa College of Law (J.D., 2021)
    • Northeastern State University (B.G.S., summa cum laude)
      • University of Oklahoma College of Pharmacy (Pharm.D.)

        Bar Admission

        • Kansas, 2026
        • Missouri, 2021

        Professional Affiliations

        • American Health Lawyers Association (AHLA)
        • American Society for Pharmacy Law (ASPL)

        Recognition

        • Adjunct professor at University of Kansas School of Pharmacy
          • Co-teaching course on pharmacy law
        • Named one of Best Lawyers: Ones to Watch® in America in Health Care Law, 2025-2026
        Publications
        Not Just a Form: Eleventh Circuit Upholds CMS-855 Conviction, Expanding Medicare Enrollment Risk
        Key Takeaways: The Eleventh Circuit recently upheld a surgeon’s conviction, prison sentence and forfeiture for false ownership disclosures on a CMS-855 Medicare enrollment form, reinforcing that inaccurate enrollment information can carry criminal consequences. The court confirmed that CMS-855 accuracy is not limited to initial enrollment but extends to every submission, including routine updates and revalidations. Providers and suppliers should implement robust CMS-855 verification and oversight controls across all submissions, with a focus on accuracy, consistency and accountability. The U.S. Court of Appeals for the Eleventh Circuit recently upheld an orthopedic surgeon’s conviction, nearly three-year prison sentence and forfeiture of $125,000 for making a false statement, in violation of 18 U.S.C. § 1035, on a Medicare enrollment application.1 This case underscores how false ownership disclosures by
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        Tiny Chains, Big Changes? What FDA’s Latest Actions Mean for Peptide Compounding
        Key Takeaways: FDA will convene the Pharmacy Compounding Advisory Committee (PCAC) on July 23-24, 2026, to discuss seven peptides for potential inclusion on the 503A bulks list. An additional five peptides will be considered at a PCAC meeting to be held before the end of Feb. 2027. FDA separately announced on April 15, 2026, that these same substances will be removed from 503A Category 2 after seven calendar days because the nominations were withdrawn, although the agency confirmed it was still planning to bring them to PCAC. That procedural removal should not be read as a go-ahead to compound these peptides. Under FDA's current policy, removal of a bulk drug substance from Category 2 does not, on its own, authorize use of that
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