Sustainability Accounting Standards Board (SASB) index
Health Care Sector
Biotechnology and Pharmaceuticals Industry
The Novartis Sustainability Accounting Standards Board (SASB) Index aligns with the Biotechnology and Pharmaceutical Industry guidelines. Data and information disclosed are sourced from the Novartis 2020 Corporate Reporting suite (Annual Review; Annual Report/Form 20-F; Novartis in Society ESG Report), and Novartis public policies and positions.
SASB indicator |
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Novartis references |
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HC-BP-210a.1 |
Discussion, by world region, of management process for ensuring quality and patient safety during clinical trials |
We have mechanisms in place to protect all trial participants when consenting to the research, during the conduct of the trial, and after completion. We have additional processes in place to protect vulnerable patients. We ensure voluntary informed consent to the research, including the right to withdraw from the trial at any time and the right to withdraw consent for the collection and use of their personal data. |
HC-BP-210a.2 |
Discussion, by world region, of management process for ensuring quality and patient safety during clinical trials |
Novartis received six FDA inspections for which one resulted in a Form 483. In each case, corrective and preventative actions were taken. |
HC-BP-210a.3 |
Total amount of monetary losses as a result of legal proceedings associated with clinical trials in developing countries |
All material legal proceedings are disclosed within the Annual Report and accounts (p.F-49). |
SASB indicator |
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Novartis references |
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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 |
Being part of the solution on pricing and access |
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 tuberculosis and malaria products on the WHO List of Prequalified Medicinal Products. |
SASB indicator |
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Novartis references |
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HC-BP-240b.1 |
Number of settlements of Abbreviated New Drug Application (ANDA) litigation that involved payments and/or provisions to delay bringing an authorized generic product to market for a defined time period |
Not reported |
HC-BP-240b.2 |
Percentage change in: |
We report these changes annually within our Novartis in Society US Report. |
HC-BP-240b.3 |
Percentage change in: |
Not reported |
SASB indicator |
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Novartis references |
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HC-BP-250a.1 |
List of products listed in the Food and Drug Administration’s (FDA) MedWatch Safety Alerts for Human Medical Products database |
Available via FDA Adverse Event Reporting website |
HC-BP-250a.2 |
Number of fatalities associated with products as reported in the FDA Adverse Event Reporting System |
Available via FDA Adverse Event Reporting website |
HC-BP-250a.3 |
Number of recalls issued, total units recalled |
In 2020, Novartis initiated 27 recalls (vs. 29 in 2019 and 42 in 2018). |
HC-BP-250a.4 |
Total amount of product accepted for takeback, reuse, or disposal |
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HC-BP-250a.5 |
Number of FDA enforcement actions taken in response to violations of current Good Manufacturing Practices (cGMP), by type |
SASB indicator |
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Novartis references |
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HC-BP-260a.1 |
Description of methods and technologies used to maintain traceability of products throughout the supply chain and prevent counterfeiting |
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HC-BP-260a.2 |
Discussion of process for alerting customers and business partners of potential or known risks associated with counterfeit products |
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HC-BP-260a.3 |
Number of actions that led to raids, seizure, arrests, and/or filing of criminal charges related to counterfeit products |
We investigated 247 incidents of suspected falsified medicines, which led to 60 successful enforcement actions and the seizure of 1.7 million medicines unit dosage forms) by law enforcement and health authorities. |
SASB indicator |
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Novartis references |
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HC-BP-270a.1 |
Total amount of monetary losses as a result of legal proceedings associated with false marketing claims |
All material legal proceedings are disclosed within the Annual Report and accounts (p.F-49). |
HC-BP-270a.2 |
Description of code of ethics governing promotion of off-label use of products |
Procedures for off-label requests outlined; further information on ethical marketing contained in Professional Practices Policy (p.5) on Promotional and Non-Promotional Materials |
SASB indicator |
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Novartis references |
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HC-BP-330a.1 |
Discussion of talent recruitment and retention efforts for scientists and research and development personnel |
Strengthening health systems |
HC-BP-330a.2 |
(1) Voluntary and (2) involuntary turnover rate for: |
Voluntary/overall turnover rate: 5.2%/10.1%; high performers voluntary turnover rate: 4.2% |
SASB indicator |
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Novartis references |
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HC-BP-430a.1 |
Percentage of (1) entity’s facilities and (2) Tier 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 |
(1) For the manufacture of medical devices, we hold the relevant certifications from ISO and other notified bodies. For all manufacturing, supply and distribution of Novartis pharmaceutical products, we hold the relevant manufacturing licenses and GMP/GxP certificates issued by the appropriate health authorities (FDA, EMEA, WHO, SwissMedic), that confirm after inspection that our duties, including our quality management systems, comply with their regulatory requirements. |
SASB indicator |
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Novartis references |
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HC-BP-510a.1 |
Total amount of monetary losses as a result of legal proceedings associated with corruption and bribery |
All material legal proceedings are disclosed within the Annual Report and accounts (p.F-49). |
HC-BP-510a.2 |
Description of code of ethics governing interactions with health care professionals |
Professional Practices Policy (p.5) |
SASB indicator |
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Novartis references |
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HC-BP-000.A |
Number of patients treated |
769 million |
HC-BP-000.B |
Number of drugs (1) in portfolio and (2) in research and development (Phases 1-3) |
(1) Novartis Global Product Portfolio (Novartis Innovative Medicines) |