340B Resource Center
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The 340B Rebate Model Pilot Drug List Is Official: 10 Manufacturers, 21 Drugs, and What FQHCs Must Do Before January 1
Read Resource →: The 340B Rebate Model Pilot Drug List Is Official: 10 Manufacturers, 21 Drugs, and What FQHCs Must Do Before January 1By Purnank Gandhi, PharmD, Founder & CEO of GapRx HRSA has approved rebate-model plans from 10 manufacturers, with an effective date of January 1, 2027. For…
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7 Mistakes You’re Making with 45-Day 340B ESP Submissions (and How to Fix Them)
Read Resource →: 7 Mistakes You’re Making with 45-Day 340B ESP Submissions (and How to Fix Them)Review frequent 45-day ESP submission mistakes that can lead to pricing access problems, and learn how stronger file preparation, validation, timing, and follow-up can reduce avoidable…
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The Ultimate Guide to FQHC File Formatting for 340B ESP: Stop the Constant Data Rejections
Read Resource →: The Ultimate Guide to FQHC File Formatting for 340B ESP: Stop the Constant Data RejectionsLearn how to structure and validate FQHC 340B ESP files to reduce data rejections, improve submission accuracy, and create a more reliable manufacturer compliance workflow.
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340B Portal Management 101: How to Navigate ESP, Truzo, and Kalderos Without Losing Your Mind
Read Resource →: 340B Portal Management 101: How to Navigate ESP, Truzo, and Kalderos Without Losing Your MindGet practical guidance for organizing manufacturer portal workflows across ESP, Truzo, Kalderos, and other systems while improving submission tracking, documentation, and operational consistency.
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Why 340B In-House Pharmacies Will Change the Way You Handle Manufacturer Restrictions
Read Resource →: Why 340B In-House Pharmacies Will Change the Way You Handle Manufacturer RestrictionsExplore how an in-house pharmacy can change a covered entity’s approach to manufacturer restrictions, pricing access, data requirements, prescription capture, and long-term 340B strategy.
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340B Portal Sprawl: Navigating New Manufacturer Demands for In-House and Clinic Claims
Read Resource →: 340B Portal Sprawl: Navigating New Manufacturer Demands for In-House and Clinic ClaimsExplore the growing number of manufacturer portals and data demands affecting in-house and clinic claims, with practical considerations for managing submissions, access, tracking, and compliance.
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Why New Manufacturer Data Portals Beyond ESP Will Change the Way You Manage 340B Compliance
Read Resource →: Why New Manufacturer Data Portals Beyond ESP Will Change the Way You Manage 340B ComplianceLearn how expanding manufacturer data portals are changing 340B compliance workflows and why covered entities need stronger processes for submission tracking, validation, documentation, and pricing access.
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How to Avoid the 340B Pricing Denial Trap: Mastering 45-Day ESP Data Submissions
Read Resource →: How to Avoid the 340B Pricing Denial Trap: Mastering 45-Day ESP Data SubmissionsLearn how timely, accurate 45-day ESP submissions can help prevent manufacturer pricing denials and strengthen the processes used to validate data, track files, and resolve exceptions.
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Why New Manufacturer Data Demands Will Change the Way You Run Your In-house Pharmacy
Read Resource →: Why New Manufacturer Data Demands Will Change the Way You Run Your In-house PharmacyExplore how expanding manufacturer data requirements can affect in-house pharmacy operations, pricing access, claims workflows, documentation, and the systems covered entities need to manage ongoing submissions.
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7 Mistakes You’re Making with 340B ESP Management (And How to Fix Pricing Denials)
Read Resource →: 7 Mistakes You’re Making with 340B ESP Management (And How to Fix Pricing Denials)Identify seven common ESP management mistakes that can contribute to manufacturer pricing denials and learn how better data validation, submission controls, tracking, and follow-up can reduce…
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