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Drug efficacy, In vitro and in vivo studies

Drug efficacy, In vitro and in vivo studies
Product Description

We offer a full range of studies and bioanalytical services, providing powerful tools and rigorous solutions for preclinical drug development of therapeutic candidates, advance lead compounds towards first-in- human trials, and support for ongoing clinical development

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galileo research

  • IT
  • 2023
    On CPHI since
  • 2
    Certificates
  • 1 - 24
    Employees
Company types
Contract Research Organisation (CRO)
Primary activities
Contract Research Organisation
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Specifications
  • Model
    Galileo helps Pharmaceutical Companies design the best strategy to select the lead drug candidate (small molecules, biopharmaceuticals and ATMPs), thus effectively accelerating the development of new medicines and reducing attrition rate.
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galileo research

  • IT
  • 2023
    On CPHI since
  • 2
    Certificates
  • 1 - 24
    Employees
Company types
Contract Research Organisation (CRO)
Primary activities
Contract Research Organisation
View company profile

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    Galileo Research can drive the nonclinical development of your medical device by preparing the Literature Report and the Biological Evaluation Plan (BEP) according to ISO 10993-1, performing additional tests, if needed, and releasing the Biological Evaluation Report (BER).

    All tests can be condu...
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    Product Consultancy for drug/MD/food development

    Our expertise offered in regulatory submissions and knowledgeable strategic skills in planning non-clinical testing programmes can reduce attrition rate and speed up the process.

  • Drug safety, in vitro and In vivo studies

    Product Drug safety, in vitro and In vivo studies

    In support of human clinical trials and marketing authorization approval, Galileo Research offers a full battery of toxicity studies for the regulatory development of small drugs, as well as biologics and advanced therapies, in compliance with Good Laboratory Practice (GLP), ICH and OECD guidelines.

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    Product Food safety evaluation

    Potential benefits and safety of dietary supplements need to be assessed by scientifically validated means, in the context of Regulation (EC) 2015/2283 on novel foods. Toxicological data, including genotoxicity, information on absorption, distribution, metabolism and excretion (ADME) need to be collecte...

galileo research resources (2)

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