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USA: 45-1 Ramsey Road, Shirley, NY 11967, USA
Europe: Heidenkampsweg 58, 20097 Hamburg, Germany
Call us at:
USA: 1-631-381-2994
Europe: 44-207-097-1828
Fax: 1-631-207-8356

In Vitro Safety Evaluation for Cancer Vaccine

It is essential to ensure the safety of vaccines. In vitro safety assessment is a prerequisite for transferring candidate vaccines from laboratory to clinical practice, including product characterization, toxicology, adjuvant toxicity and stability, immunogenicity studies, and all aspects of microbial contamination testing. Creative Biolabs offers a range of pre-clinical in vitro tests to ensure these key attributes.

Evaluation Category

Creative Biolabs' safety assessments are conducted in the following categories:

  1. Novel adjuvant
  2. Vaccine adjuvants
  3. Vaccine antigen
  4. Adjuvanted vaccines
  5. General vaccines

In Vitro Safety Evaluation Service

In vitro safety studies conducted prior to the start of clinical trials (pre-clinical) identified potential safety issues and helped prevent possible harm to humans. Potential problems include toxicity caused by active ingredients or excipients, reactions to trace impurities (e.g., production substrates), and interactions between other vaccine components administered simultaneously.

In vitro safety assessment that Creative Biolabs includes:

  • Inherent toxicity caused directly by vaccine ingredients
  • Intrinsic toxicity associated with excipients, adjuvants or preservatives in the formulation
  • Cross-reactivity between candidate vaccine autoantigens and antibodies produced by vaccines
  • Contaminants and impurities
  • Genotoxicity testing
  • Cytotoxicity testing
  • In vitro carcinogenicity
  • Efficacy evaluation

With our professional team of experts, Creative Biolabs is dedicated to helping you identify the most promising candidate vaccines to help you enter the post-development phase.

For more details, please feel free to contact us for project quotations and more detailed information.

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