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In our latest article, we look beyond the vote and examine what comes next, including: • The rulemaking process FDA would need to undertake • How long that process could take—and why delay itself matters • Whether FDA could reconsider its interim enforcement posture • What pharmacies should and should not be doing now • How the industry can strengthen the scientific and administrative record • The potential role of Congressional advocacy • Why proposing meaningful regulatory guardrails may ultimately be more effective than simply asking FDA for unrestricted access One point is particularly important: the industry should not simply wait for FDA