Sustainability Accounting Standard Board (SASB) index 2025
The Novartis SASB index aligns with the Biotechnology & Pharmaceuticals Sustainability Accounting Standard (industry standard | version 2023-12). Information referenced has been sourced from our Report on Nonfinancial Matters, Annual Report/Form 20-F, ESG Data Summary, corporate website, Novartis public policies and positions, and public databases or selected materials from third parties where applicable. For additional information about our ESG practices, please visit https://www.novartis.com/esg.
Disclosure | Reference | |
Safety of Clinical Trial Participants | ||
HC-BP-210a.1 | Discussion, by region, of management process for ensuring quality and patient safety during clinical trials | Report on Nonfinancial Matters 2025, page 34 Novartis commitment to patients and caregivers Human Rights Commitment Statement Ethics in Clinical Trials |
HC-BP-210a.1 | Number of inspections related to clinical trial management and pharmacovigilance that resulted in: (1) entity voluntary remediation or (2) regulatory or administrative actions taken against the entity | ESG Index: quality and supply ESG Data Summary 2025, page 2 |
HC-BP-210a.1 | Total amount of monetary losses as a result of legal proceedings associated with clinical trials in developing countries | All significant legal proceedings are disclosed within the Annual Report and accounts (Annual Report 2025, Item 18. Note 20) |
Access to Medicines | ||
HC-BP-240a.1 | Description of actions and initiatives to promote access to health care products for priority diseases and in priority countries as defined by the Access to Medicine Index | Report on Nonfinancial Matters 2025, page 35 Access to Medicine Index 2024 |
HC-BP-240a.2 | List of products on the WHO List of Prequalified Medicinal Products as part of its Prequalification of Medicines Programme (PQP) | Novartis has malaria products on the WHO List of Prequalified Medicinal Products |
Affordability & Pricing | ||
HC-BP-240b.2 | Percentage change in: (1) weighted average list price and (2) weighted average net price across product portfolio compared to previous reporting period | Not reported |
HC-BP-240b.3 | Percentage change in: (1) list price and (2) net price of product with largest increase compared to previous reporting period | Not reported |
Drug Safety | ||
HC-BP-250a.1 | Products listed in public medical product safety or adverse event alert databases | Available via FDA Adverse Event Reporting System (openFDA) |
HC-BP-250a.2 | Number of fatalities associated with products | Available via FDA Adverse Event Reporting System (openFDA) |
HC-BP-250a.3 | (1) Number of recalls issued, (2) total units recalled | Report on Nonfinancial Matters 2025, page 35 |
HC-BP-250a.4 | Total amount of product accepted for takeback, reuse, or disposal | Report on Nonfinancial Matters 2025, page 35 |
HC-BP-250a.5 | Number of enforcement actions taken in response to violations of good manufacturing practices (GMP) or equivalent standards, by type | ESG Index: quality and supply ESG Data Summary 2025, page 2 |
Sustainability Accounting Standard Board (SASB) index 2025
Disclosure | Reference | |
Counterfeit Drugs | ||
HC-BP-260a.1 | Description of methods and technologies used to maintain traceability of products throughout the supply chain and prevent counterfeiting | ESG Index: quality and supply Novartis Position on Falsified Medical Products |
HC-BP-260a.2 | Discussion of process for alerting customers and business partners to potential or known risks associated with counterfeit products | ESG Index: quality and supply |
HC-BP-260a.3 | Number of actions that led to raids, seizure, arrests, or filing of criminal charges related to counterfeit products | ESG Index: quality and supply |
Ethical Marketing | ||
HC-BP-270a.1 | Total amount of monetary losses as a result of legal proceedings associated with false marketing claims | All significant legal proceedings are disclosed within the Annual Report and accounts (Annual Report 2025, Item 18. Note 20) |
HC-BP-270a.2 | Description of code of ethics governing promotion of off-label use of products | Report on Nonfinancial Matters 2025, page 37 The Novartis Code of Ethics Doing Business Ethically Policy |
Employee Recruitment, Development & Retention | ||
HC-BP-330a.1 | Discussion of talent recruitment and retention efforts for scientists and research and development staff | Careers in research and development US Biomedical Research internship programs |
HC-BP-330a.2 | (1) Voluntary and (2) involuntary turnover rate for: (a) executives/senior managers, (b) mid-level managers, (c) professionals, and (d) all others | Report on Nonfinancial Matters 2025, page 12 |
Supply Chain Management | ||
HC-BP-430a.1 | Percentage of (1) entity's facilities and (2) Tier I suppliers' facilities participating in the Rx-360 International Pharmaceutical Supply Chain Consortium audit program or equivalent third-party audit programs for integrity of supply chain and ingredients | Novartis quality management system (QMS) External Partner Risk Management (EPRM) ESG Data Summary 2025, page 2 |
Business Ethics | ||
HC-BP-510a.1 | Total amount of monetary losses as a result of legal proceedings associated with corruption and bribery | All significant legal proceedings are disclosed within the Annual Report and accounts (Annual Report 2025, Item 18. Note 20) |
HC-BP-510a.2 | Description of code of ethics governing interactions with health care professionals | Report on Nonfinancial Matters 2025, page 38 The Novartis Code of Ethics Doing Business Ethically Policy |
Activity Metrics | ||
HC-BP-000.A | Number of patients treated | Report on Nonfinancial Matters 2025, page 36 |
HC-BP-000.B | Number of drugs (1) in portfolio and (2) in research and development (Phases 1-3) | Products ESG Data Summary 2025, page 2 |
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Novartis AG published this content on February 09, 2026, and is solely responsible for the information contained herein. Distributed via Public Technologies (PUBT), unedited and unaltered, on February 09, 2026 at 14:22 UTC.


















