Our Sustainability Accounting Standards Board (SASB) Index discloses information in alignment with SASB’s Health Care Delivery and Medical Equipment & Supplies standards. This reflects our commitment to providing transparent and relevant information on our economic, environmental- and social performance to our stakeholders.
Where questions require specific information related our U.S. business operations, this is indicated in the information provided.
| SASB Code | Accounting Metric | Response / Sources | |
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Health Care Delivery |
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| Energy Management | |||
| HC-DY-130a.1 | (1) Total energy consumed, (2) percentage grid electricity, (3) percentage renewable | (1) 10,768,176 GJ (3 million MWh)
For further information on energy management, see chapter "Climate Change" in our Sustainability Statement. |
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| Waste Management | |||
| HC-DY-150a.1 | Total amount of medical waste, percentage (a) incinerated, (b) recycled or treated, and (c) landfilled | We report data on waste as well as recycling and treatment methods in the Sustainability Statement. Note: Reported waste figures do not exclusively cover medical and pharmaceutical waste but encompass all waste generated across our operations. . For an overview of our waste treatment methods, please see chapter "Resource Use and Circular Economy" in our Sustainability Statement. |
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| HC-DY-150a.2 | Total amount of: (1) hazardous and (2) nonhazardous pharmaceutical waste, percentage (a) incinerated, (b) recycled or treated, and (c) landfilled | ||
| Patient Privacy & Electronic Health Records | |||
| HC-DY-230a.2 | Description of policies and practices to secure customers’ protected health information (PHI) records and other personally identifiable information (PII) | Fresenius Medical Care manages patients’ personal information in full alignment with its Global Privacy Principles. For every processing activity — including collection, access, use, sharing, or transfer of personal data — we carefully assess the scope, purpose, and legal basis to ensure compliance with applicable privacy laws and internal policies.
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| HC-DY-230a.3 | (1) Number of data breaches, (2) percentage involving (a) personally identifiable information (PII) only and (b) protected health information (PHI), (3) number of customers affected in each category, (a) PII only and (b) PHI | In 2025, Fresenius Medical Care received 718 internal reports related to data. 155 of these were reportable data breaches, as defined by appliable laws and procedures. Out of the total number, 119 (16.57%) were in relation to PHI (Personal Health Information) and 599 (83.43%) in relation to PII (Personal Identifiable Information). | |
| HC-DY-230a.4 | Total amount of monetary losses as a result of legal proceedings associated with data security and privacy | Fresenius Medical Care did not incur monetary losses during the reporting period as a result of legal proceedings associated with data security and privacy, (meaning any adjudicative proceedings before a court, regulator, arbitrator or otherwise). |
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| Access for Low-Income Patients | |||
| HC-DY-240a.1 | Discussion of strategy to manage the mix of patient insurance status | In our dialysis clinics, we treat patients with all kinds of insurance status. In the United States, the insurance mix includes the federal health insurance programs Medicare and Medicaid, as well as private/alternative payors such as commercial insurance and private funds.
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| Quality of Care & Patient Satisfaction | |||
| HC-DY-250a.2 | Number of Serious Reportable Events (SREs) as defined by the National Quality Forum (NQF) | We do not report this data. For information on quality of care and patient satisfaction, see chapter "Patients" in our Sustainability Statement. | |
| HC-DY-250a.3 | Hospital-Acquired Condition (HAC) Score per hospital | We do not operate acute care hospitals in the United States. Consequently, this indicator is not relevant for us. | |
| HC-DY-250a.6 | Number of (1) unplanned and (2) total readmissions per hospital | We do not operate acute care hospitals in the United States. Consequently, this indicator is not relevant for us. | |
| Management of Controlled Substances | |||
| HC-DY-260a.1 | Description of policies and practices to manage the number of prescriptions issued for controlled substances | The United States (US) dialysis services business does not permit controlled substances to be kept or administered in its outpatient dialysis units. Nephrologists and other providers cannot prescribe controlled substances to be administered to patients as part of the dialysis treatment. |
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| Pricing & Billing Transparency | |||
| HC-DY-270a.1 | Description of policies or initiatives to ensure that patients are adequately informed about price before undergoing a procedure | All of FME’s Care Delivery patient facing services businesses (e.g. in the U.S. Fresenius Kidney Care’s in-center, home dialysis, Azura Vascular, FRx as well as Nephrocare in EMEA, and Fresenius Kidney Care in AP) follow the local laws and requirements governing pricing disclosures. The method of communication varies by country and includes written communication, website posting, and in-person consultation, as required. The insurance provider informs the business about what the patient is responsible for based on their plan. In the case of self-pay patients, the business can provide an estimate of price. |
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| HC-DY-270a.2 | Discussion of how pricing information for services is made publicly available | For the US Care Delivery patient facing services business (e.g. Fresenius Kidney Care’s in-center, home dialysis as well as Azura Vascular), the Company sets our pricing and certain pricing information is made publicly available. |
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| HC-DY-270a.3 | Number of the entity’s 25 most common services for which pricing information is publicly available, percentage of total services performed (by volume) that these represent | Pricing transparency requirements in the U.S. are for hospitals and not required for other health facilities. https://www.cms.gov/priorities/key-initiatives/hospital-price-transparency/hospitals |
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| Employee Health & Safety | |||
| HC-DY-320a.1 | Total recordable incident rate (TRIR) for (a) direct employees and (b) contract employees | (a) For the total recordable incident rate, see chapter "Working for Fresenius Medical Care" in our Sustainability Statement.
(b) We do not report the total recordable incident rate for contract employees. For further information on employee health and safety, see chapter "Working for Fresenius Medical Care" in our Sustainability Statement. |
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| Employee Recruitment, Development & Retention | |||
| HC-DY-330a.1 | (1) Voluntary and (2) involuntary turnover rate for: (a) physicians, (b) non-physician health care practitioners, and (c) all other employees | For 2025, our total voluntary turnover rate is 15.6%, and our total involuntary turnover rate is 5.2%. |
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| HC-DY-330a.2 | Description of talent recruitment and retention efforts for health care practitioners | For information on recruitment and retention efforts, see our Sustainability Statement, chapter "Working for Fresenius Medical Care", our global career website, and our employee website. For information on nurses training programs, global career paths, and insights into the jobs of our clinical staff, see our Nephrocare website and our corporate website. |
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| Climate Change Impacts on Human Health & Infrastructure | |||
| HC-DY-450a.1 | Description of policies and practices to address: (1) the physical risks due to an increased frequency and intensity of extreme weather events and (2) changes in the morbidity and mortality rates of illnesses and diseases, associated with climate change and (3) emergency preparedness and response |
1) Fresenius Medical Care takes steps to ensure the continuous operation of our critical healthcare services through providing backup power systems. For our U.S. dialysis clinics, we have placed back-up built-in power generators in areas in the southeast which are most prone to hurricanes. For our EMEA, AP, and some U.S. dialysis, there is a requirement that back up and built-in power generators be available where required by law. Our ambulatory surgery centers, pharmacy, and lab businesses also have facility generators as standard. |
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| Fraud & Unnecessary Procedures | |||
| HC-DY-510a.1 | Total amount of monetary losses as a result of legal proceedings associated with Medicare and Medicaid fraud under the False Claims Act | The United States business did not sustain any monetary losses as a result of such proceedings during the reporting period. | |
Medical Equipment and Supplies |
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| Affordability & Pricing | |||
| HC-MS-240a.2 | Description of how price information for each product is disclosed to customers or to their agents | The business makes certain pricing information publicly available where required by price transparency laws. Pricing is usually subject to local law and reimbursements. | |
| HC-MS-240a.3 | Percentage change in: (1) weighted average list price and (2) weighted average net price across product portfolio compared to previous reporting period | ||
| Product Safety | |||
| HC-MS-250a.1 | (1) Number of recalls issued, (2) total units recalled | In the United States, there were five recalls of drugs and devices in 2025 in the form of removals, corrections, alerts or safety notices. In non-U.S. markets, there were five recalls of medical devices and one recall of medicinal products in 2025. |
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| HC-MS-250a.2 | List of products listed in the FDA’s MedWatch Safety Alerts for Human Medical Products database | None of our products were newly listed in FDA’s MedWatch Safety Alerts for Human Medical Products database in 2025. | |
| HC-MS-250a.3 | Number of fatalities associated with products | No fatalities have been reported in which a causal relationship with our products has been definitively established. |
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| HC-MS-250a.4 | Number of enforcement actions taken in response to violations of good manufacturing practices (GMP) or equivalent standards, by type | In 2025, the FDA issued a Regulatory Meeting Request Letter on January 8, 2025. FME has committed to implementing short term and long-term actions to address regulatory compliance concerns. Corrective and preventive actions have been implemented to address the 2024 and 2023 Warning Letter. We continue to work on quality system improvements. | |
| Ethical Marketing | |||
| HC-MS-270a.1 | Total amount of monetary losses as a result of legal proceedings associated with false marketing claims | All relevant legal proceedings and related financial effects are disclosed in our Annual Report – Notes to the consolidated financial statements. None of these were associated with false marketing claims which resulted in monetary losses. | |
| HC-MS-270a.2 | Description of code of ethics governing promotion of off-label use of products | Our Code of Ethics and Business Conduct outlines our commitment always to be truthful, accurate, and not misleading when promoting our products and services. For further information on advertising and promotion, see our Code of Ethics and Business Conduct – Advertising and promotion. | |
| Product Design & Lifecycle Management | |||
| HC-MS-410a.1 | Discussion of process to assess and manage environmental and human health considerations associated with chemicals in products, and meet demand for sustainable products | It is essential that our products and services are effective, reliable, and associated with minimal risk to patients. Robust standards for the planning, conduct, and monitoring of clinical studies underpin the quality and safety of our products. The product assessment integrates relevant criteria, including circular economy principles and material use for our products and packaging. Through simplified life cycle assessments (screening-LCAs), we measure and compare the environmental impacts of our products, covering factors such as critical materials, energy consumption, and end-of-life pathways. Currently, screening LCAs are conducted for a majority of our current medical device product lines. We have conducted detailed comparative LCAs for selected disposable products to validate findings and guide material and process improvements |
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| HC-MS-410a.2 | Total amount of products accepted for take-back and reused, recycled, or donated, broken down by: (1) devices and equipment and (2) supplies | Globally, we donate dialysis machines and medical supplies to organizations that require support. In 2025 we donated approximately 1.9 metric tons of devices and equipment reflecting a total value of around 12, 700 €. We also donated approximately 3.94 metric tons of supplies reflecting a total value of around 1,240,000 €. Most of the products/supplies donated reflect a partnership FME started with an organization called Supporting Initiatives to Redistribute Unused Medicine (SIRUM), where we donated unused, unexpired, non-controlled, and non-refrigerated medications. SIRUM will take our donations and redistribute to people in need through community clinics and charitable pharmacies in the United States. We also continued our program for reusing blue drums that are used to deliver acid concentrate to clinics in the U.S. In 2025, we reused more than 900 metric tons of drums. The drums are collected at care centers. They then go through a cleaning process at the production site making them suitable for reuse. |
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| Supply Chain Management | |||
| HC-MS-430a.1 | Percentage of (1) entity's facilities and (2) Tier I suppliers' facilities participating in third-party audit programs for manufacturing and product quality | Not applicable. | |
| HC-MS-430a.2 | Description of efforts to maintain traceability within the distribution chain | As part of our digitalization strategy, we implemented an integrated software solution which assist in automating global transactions and enabling compliant supplier onboarding and monitoring, as well as significantly enhancing supply chain transparency. We have mapped our value chain, focusing on both tier 1 suppliers and sales intermediaries. We collect data relating to country where supplier is located, industry of the supplier regarding products delivered, Fresenius Medical Care internal procurement category and spend. The information is, for example, used for the supplier risk assessment in line with the German Act on Corporate Due Diligence in Supply Chains (LkSG). For Sales Intermediaries, we have a dedicated business team. Our compliance organization also conducts due diligence activities and specific audits. | |
| HC-MS-430a.3 | Description of the management of risks associated with the use of critical materials | Responsible sourcing of mineral raw materials remains a key part of our commitment to sustainable procurement. We acknowledge that mineral extraction, especially in high-risk regions, may be associated with poor labor practices and human rights violations. We adhere to Section 1502 of the U.S. Dodd-Frank Wall Street Reform and Consumer Protection Act, which addresses the use of “conflict minerals”. Our approach is guided by the OECD Due Diligence Guidance for Responsible Supply Chains of Minerals from Conflict-Affected and High-Risk Areas, as outlined in our Conflict Minerals Policy. We publish an annual conflict minerals report. Suppliers found to be non-compliant with our Conflict Minerals Policy are subject to review for ongoing business engagement. We actively encourage our suppliers to foster similar standards and promote transparency within their own supply chains.
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| Business Ethics | |||
| HC-MS-510a.1 | Total amount of monetary losses as a result of legal proceedings associated with bribery or corruption | We had no monetary losses associated with formal legal proceedings associated with bribery or corruption in 2024. All relevant legal proceedings and related financial effects are disclosed in our Annual Report – Notes to the consolidated financial statements. |
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| HC-MS-510a.2 | Description of code of ethics governing interactions with health care professionals | As a healthcare company, we interact with external (third-party) healthcare professionals (HCPs) and patient organizations. The responsibility for patient treatment lies with HCPs who must be able to make independent clinical decisions. Our global HCP Policy governs interactions with third-party HCPs and establishes safeguards. The policy is overseen by the Compliance department and is available to all employees. |
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