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FDA stem cells (view source)

Revision as of 03:59, July 13, 2023

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{{cquote|Because the plain text of the regulation suggests that "such HCT/Ps" must be in their original form (rather than subjected to extensive processing), and because this understanding is confirmed by the agency's contemporaneous statements and its later, thoroughly-considered interpretation, we hold the same surgical procedure exception unambiguously does not apply to the Clinic's procedure. The stromal-vascular fraction solution is the product of an intensive cell isolation process involving enzymatic digestion that goes much farther than simple rinsing or sizing. By the time the stromal-vascular fraction is reinjected, it is no longer "such HCT/P" as the adipose tissue removed from the patient.}}
 
{{cquote|Because the plain text of the regulation suggests that "such HCT/Ps" must be in their original form (rather than subjected to extensive processing), and because this understanding is confirmed by the agency's contemporaneous statements and its later, thoroughly-considered interpretation, we hold the same surgical procedure exception unambiguously does not apply to the Clinic's procedure. The stromal-vascular fraction solution is the product of an intensive cell isolation process involving enzymatic digestion that goes much farther than simple rinsing or sizing. By the time the stromal-vascular fraction is reinjected, it is no longer "such HCT/P" as the adipose tissue removed from the patient.}}
 
''United States v. US Stem Cell Clinic, Ltd. Liab. Co.'', 998 F.3d 1302, 1310 (11th Cir. 2021)
 
''United States v. US Stem Cell Clinic, Ltd. Liab. Co.'', 998 F.3d 1302, 1310 (11th Cir. 2021)
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=== District Court ===
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The district court did not rely on a guidance by the FDA:
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{{cquote|In conclusion, the Guidance is not, by its terms [**36]  or by the FDA's interpretation, "legally binding" and, even if the FDA considered it as such, it would be irrelevant to the disposition of this action. ''See'' ''United States v. Regenerative Scis., LLC'', 741 F.3d 1314, 1322, 408 U.S. App. D.C. 259 (D.C. Cir. 2014) ("Appellants claim that the FDA seeks to give legal effect to a statement that was not promulgated through formal rule-making procedures . . . Our decision, however, is based on, and gives effect to, the Part 1271 Regulations, not the preamble. Appellants' procedural challenge to the preamble is therefore irrelevant."). Congress has delegated to the FDA substantial discretion in the regulation of drugs and biological products, its interpretation of § 1271.15(b) is neither facially inconsistent nor otherwise plainly erroneous and is historically consistent with the FDA's position regarding the regulation of HCTP's. Therefore, the FDA's interpretation of the same surgical procedure exception in 21 C.F.R. § 1271.15(b) is entitled to deference under Auer.9 519 U.S. 452, 117 S. Ct. 905, 137 L. Ed. 2d 79. Under this interpretation, "such HCT/P" implanted into the patient refers to all of the HCT/P removed from the patient in its original form, subject to limited handling. As Defendants' SVF therapy extracts adipose tissue, but only implants the SVF into the patient, after subjecting it to a specific and complex multi-step procedure, the HCT/P is no longer in its original form. Thus, the same surgical procedure exception does not and cannot apply to Defendants as a matter of law, and they are therefore subject to FDA regulation. As this is the sole issue on which Defendants move for summary judgment, the Court denies Defendants' Motion and grants the FDA's Motion on this issue.}}
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''United States v. US Stem Cell Clinic, LLC'', 403 F. Supp. 3d 1279, 1296 (S.D. Fla. 2019).
    
== Analogous therapies ==
 
== Analogous therapies ==
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