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We provide you with everything you need to know about our products so that you can properly inform and treat your patients: how they are manufactured and shipped, indications, potential side effects, storage and use, training and documentation, and ongoing support. We answer your questions, find solutions and deliver on what we promise.
Remsima® is a biosimilar anti-TNF alpha used in rheumatology and gastro-enterology. Developed by Celltrion Healthcare, it was approved for sale in Switzerland in 2015. It is a Class A drug that must be stored between 2°C and 8°C. Remsima is administered intravenously.
Remsima-infliximab 100mg
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Veblocema® is an anti-TNF alpha antibody used in gastro-enterology and rheumatology which has been approved in Switzerland as an innovative product. Developed by Celltrion Healthcare, it was added to the specialty list in July 2022. It is a Class A drug that must be stored between 2°C and 8°C. First of its kind, Veblocema’s infliximab is administered subcutaneously.
Veblocema-infliximab 120mg
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Yuflyma® is a biosimilar anti-TNF alpha used in rheumatology, gastro-enterology, dermatology & ophtalmology. Developed by Celltrion Healthcare, it was approved in Switzerland in 2022. It is a Class B drug that must be stored between 2°C and 8°C. Yuflyma is administered subcutaneously and is available in prefilled pen and prefilled syringe with needle guard.
Yuflyma-adalimumab 40mg/0.4ml and 80mg/0.8ml
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Truxima® is a biosimilar monoclonal antibody designed to target the CD20 antigen. It was developed by Celltrion Healthcare for use in hematology, rheumatology and oncology, and received market approval in Switzerland in 2019. It is a Class A drug that must be stored between 2°C and 8°C. Truxima® is administered intraveneously.
Truxima-rituximab 100mg and 500mg
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Herzuma® is a biosimilar monoclonal antibody designed to target HER2. It was developed by Celltrion Healthcare for use in oncology and received market approval in Switzerland in 2021. It is a Class A drug that must be stored between 2°C and 8°C. Herzuma® is administered intravenously.
Herzuma-trastuzumab 150mg and 440mg
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Vegzelma™ is a biosimilar monoclonal antibody designed to target VEGF-A. It was developed by Celltrion Healthcare for use in oncology and received market approval in Switzerland in 2023. It is a Class A drug that must be stored between 2°C and 8°C. Vegzelma™ is administered intravenously.
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Grasustek® is a biosimilar granulocyte colony stimulating factor used in oncology. Developed by USV Private Limited, it was approved for sale in Switzerland in 2021. It is a Class A drug that must be stored between 2°C and 8°C. Grasustek® can be self-administered subcutaneously.
Grasustek-pegfilgrastim 6mg
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Idefirix® is indicated for desensitization treatment in kidney transplant. Developed by the Swedish company Hansa Biopharma, Idefirix contains the novel active substance imlifidase. Idefirix is administered intravenously and for hospital use only.
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What is the difference between a biosimilar and an original?
An original biologic is a complex product generated from biotechnological processes within living cells. A biosimilar is similar to the original biologic but only appears on the market after the reference product is no longer protected by a patent. A biosimilar is "similar" to the original in terms of efficacy, safety and quality, as well as in the clinical sense; very slight variations can occur, however, because biosimilars are produced by living systems (cells).
How effective is a biosimilar compared to the reference product?
They are equally effective, as shown by repeated clinical trials and as certified by Swissmedic. Because of their biological origin, biosimilars may vary slightly from one production run to the next, but any variations remain within very precise limits and in no way influence the products’ safety, efficacy and quality.
Is there a price difference between a biosimilar and the original? Is the biosimilar reimbursed by insurance companies?
According to the Swiss Federal Office of Public Health (FOPH), biosimilars must generally cost at least 25% less than their reference products when they are marketed (with some exceptions). Biosimilars are reimbursed by insurance companies in exactly the same way as their reference products.
How and why should I use a biosimilar instead of the original? Why should I switch?
The significant price difference between biosimilars and originals leads to significant savings and enhances the financial efficiency of our healthcare system. This means that more people can benefit from modern therapies at a reasonable price.
Where can I find additional and detailed information about your biosimilar products and their use?
For more information on our products, feel free to reach out to us or visit the Swissmedic website. You may also find useful information on our partner companies' websites.