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Salmonella vaccine development support

SSI Diagnostica Group’s involvement in vaccine development began over 40 years ago—then as Statens Serum Institut—by supplying antisera for quality control to a global vaccine manufacturer during the development of a pneumococcal vaccine. Today, SSI Diagnostica Group continues to provide leading vaccine developers, including GSK, with high-quality products and scientific expertise across multiple disease areas.  This page introduces to the products we can offer for Salmonella vaccine development. 

Overview: Current Salmonella vaccines

Salmonella is a major global health concern. Licensed vaccines for human use exist for S. Typhi (e.g., Vi polysaccharide and Ty21a oral vaccines). There are no licensed vaccines for S. Paratyphi or NTS available for humans yet, but several candidates are in clinical development, including conjugate and protein-based vaccines1

Our portfolio is structured to meet the evolving needs of vaccine developers from research & development all the way to post-market surveillance. 

 
Research and
development 

Pre-clinical 

Clinical 
studies

Production 

Post market
surveillance 
Salmonella strains 
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Salmonella antisera / Serotyping kits  
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S. Typhi/Paratyphi Ag Rapid Test
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OnSite® Typhoid IgG/IgM Combo Rapid Test 
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Customization and contract manufacturing services

Please note
Product availability may vary by country. Some products listed in the table might not be registered or available in all markets. For detailed information on distribution and registration status in your region, please contact SSI Diagnostica Group or your local representative. 

Research & development 

  • Supporting serotype identification and discovery 
  • Supporting with consistent QC design 
  • Providing raw materials (reference strains)  

Preclinical trials 

  • Raw material and support for in-house assays 

Clinical trials 

  • IVD tests for pre-screening of study participants 
  • Raw material and support for in-house assays 

Production 

  • Scalable supply of validated reagents 

Post market surveillance 

  • Ongoing support for surveillance and refinement 

Customization and contract manufacturing services  

  • Available across all development stages
  • Trusted by leading vaccine manufacturers for 40+ years 
  • High quality IVD products (IVDD / IVDR) 
  • Stable supply by 100% in-house production
  • Global distribution (130+ countries)
  • Compliant with manufacturing, regulatory and environmental standards / requirements (ISO 13485, ISO 14001, 21 CFR 820) 

If you have any questions, comments, or collaboration inquiries, you are very welcome to reach out.

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