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for patients

Empowering patients to work alongside us and play an active role in their own health

Patients are taking more and more control of their own health. At Servier, we see this shift as a unique opportunity to work both with and for them to develop medicines that better suit their needs. 

We involve them in our work, right from the moment the molecule design process begins and at every stage of the medicine life cycle. 

Their understanding of their illnesses and the medicines they take drive our research, which in turn improves treatment and increases the effectiveness of the therapeutic solutions we develop. 

We particularly appreciate the valuable contribution made by patient organizations, from diagnosis through to properly following treatment. 

Genuine therapeutic progress comes through close collaboration with patients. 

3rd

Ranked 3rd out of 26 companies by oncology patient organizations, according to the PatientView Report 2023 on the reputation of pharmaceutical companies

12

international or European patient organizations collaborated with Servier in 2023

66%

of informed consent forms filled out by people taking part in Servier Group clinical trials were reviewed by patients in 2022-2023. We aim to reach 100% within the next three years.

100%

of our lay summaries are approved by patient representative bodies and translated into the language of every country involved in the study.

65%

of clinical research projects were reviewed by patients in 2022-2023.

With 18 patients representing ten different pathologies, the Servier Saclay Research & Development Patient Board worked with our R&D teams to integrate patients’ views even more effectively into the research and development of new drugs.

ACT for Children

Servier has joined forces with Childhood Cancer International (CCI), the IDA Foundation, the International Society of Pediatric Oncology (SIOP), Resonance, and World Child Cancer to address disparities in pediatric cancer recovery rates between high-income countries and low- and middle-income countries (LMICs), through the ACT for Children partnership. 80%(3) of children with cancer can be cured when childhood cancer services are accessible, yet only 29% of low-income countries report that cancer medicines are generally available to their populations (compared to 96% of high-income countries1).

Aligned with the WHO CureAll framework, this collaboration aims to transform the landscape of pediatric cancer care in LMICs by providing quality medical care, life-saving medications for pediatric acute lymphoblastic leukemia— the most common childhood cancer—and laying the foundation for long-term, sustainable impact. ACT for Children also works closely with the UICC (Union for International Cancer Control)-led Access to Oncology Medicines Coalition, driving a new model of equitable healthcare for children with cancer.

Four ACT for Children sites have already been set up in 2024 in Armenia, El Salvador, Guatemala, and Honduras, serving as key hubs for comprehensive care and improvement tracking. The initiative was launched on International Childhood Cancer Day 2025.

For more information, see our video and press release.

Harnessing industrial excellence and independence to benefit patients

Thanks to our network of 14 production sites located throughout the world, we produce and distribute our medicines in accordance with the highest standards on quality, safety and reliability.

As a pharmaceutical Group deeply committed to health independence, we have always actively chosen to maintain significant production capacity in Europe. That is why we produce 96.5% of our active ingredients at our Oril Industrie facility in France, before distributing them to nine production sites for use in medicines prescribed in cardiology, neuroscience and diabetes.

96,5%

of our active ingredients are produced at our Oril Industrie facility in France.

By harnessing digital innovation across the entire value chain, we continue to enhance our ability to meet patient demand.

Combating counterfeit medicine

Counterfeit medicines represent a serious risk to public health and a danger to patients, as there can be a lack of active ingredients, incorrect dosage, impurities and toxic substances.

The WHO estimates that 10% of medicines distributed in developing countries are of substandard quality or are counterfeit. Counterfeit medicine therefore represents a major cause of inequalities in treatment. 

We have been working for several decades to counter the scourge of counterfeit medicines. 

As a member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), we promote prevention, training and medicine traceability. 

In addition, our specialist teams are involved in developing innovative technology, such as electronic and near infrared product labeling which serve to analyze suspicious boxes of medicines found throughout the world.  More generally, our generic medicines help combat the problem posed by falsified medicines; as generics are less expensive than brand-name medicines, they help drive counterfeit drugs off the market.

Learn more about our commitment and actions to fight against counterfeiting.

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[1] WHO  https://www.who.int/news-room/fact-sheets/detail/cancer-in-children