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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

galileo research

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

galileo research

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

More Products from galileo research (4)

  • Biocompatibility of Medical Devices according to ISO 10993-1 series

    Product Biocompatibility of Medical Devices according to ISO 10993-1 series

    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...
  • Consultancy for drug/MD/food development

    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.

  • Food safety evaluation

    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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  • Product Clinical solutions: Trials

    Conscio's in-house clinical Unit has been operating since 2007, with more than 600 BA/BE/PK studies completed and proprietary of over 270 validated bioanalytical methods. Equipped with a 60-bed on-site clinical unit in Prague and a recently opened 36-bed unit in Ostrava, we provide comprehensive services w...
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  • Product Data Sciences

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  • Product Integrated Services

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  • Product TIM-2

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    KBI’s experienced team produces high-quality therapeutics and vaccines thro...
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  • Product Medical Device Testing

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    3) Biological Testing of Raw Material of Plastic, Rubber,Silicone, Polymers, etc.(As per IP / BP / EP / JP / USP)
    4) Microbiological Testing Services ...
  • Product R&D Services

    Our R&D Services are categorized into 8 streams: • Material Science Services

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    • Organic Synthesis Services

    • Catalysis Services

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    • Chromatography and Purification Services

    • Method D...
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  • Product Analytical Services

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  • Product Cell-based Neutralization Assays

    Experienced cell-based neutralizing antibody assay capabilities. Our experts, at our GLP/GCP compliant laboratory, evaluate each therapeutic, conduct tailored assay development and ensure that each assay is optimized to suitably determine the presence of NAb with maximum possible level of drug toleran...
  • Product Microbiology

    • Sterility Testing • Quality Control Release • Bioburden Testing • Method Suitability • Microbial Identification - MALDI-TOF • Bacterial Endotoxin Testing • Cytotoxicity • Environmental Monitoring • Biological Indicator Enumeration
  • Product Clinical Trial Design

    Study design is a significant phase of any clinical research project. At Atlantia we feel that our careful planning and guidance to our clients coupled with our extensive experience with regulation, pre diseased and diseased populations, is what brings our clients back time and again to trust us with their...
  • Product GCP Services(Good Clinical Practices)

    We offer various GCP services which can help the clients across globe, ranging from audits to monitoring services. We provide comprehensive GCP Quality Compliance services to the pharmaceutical industry. Our GCP consulting services are characterized by:

    1) Knowledge: Various regulatory requi...
  • Product Clinical Trial Services

    Our experts will accomplish your clinical objectives by leading the way from recruitment strategies, site selection, and clinical logistics, all the way through the regulatory process. 

    We use our own eClinical suite to be more cost-efficient and keep you connected remotely acros...
  • Product Regulatory Status

    Main Authorizations for Markets


    China CN FDA and Brasil ANVISA in process
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    Making Spray Dry COOL! Introducing the Future of Spray Dry & Microencapsulation.  The patent-pending PolarDry® Electrostatic Spray Dryer utilizes revolutionary electrostatic technology which drives water to the shell and active to the core, lowering the evaporation temper...
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    We offer a range of GCP services, from monitoring to audits. Providing comprehensive GCP compliance services for the pharmaceutical industry is one of our specialties.

    A.   Risk-Based Monitoring: 

    ✔ Risk-Based Monitoring for Bioequivalence/Bioavailability Studies (BE...
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    NCEs • Phase I-III formulation process development and clinical supply manufacturing Generic drugs
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  • Product BDD Scintigraphy

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  • Product Certified toxicological studies

    Toxicological tests performed at the Lukasiewicz - IPO:
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    -make it possi...
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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).

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    We design and execute clinical trials so new therapies get to market in the quickest and safest way possible. Full-Service Solution: We manage and execute full-service clinical trials across major therapeutic areas within medical device, diagnostics, drug, and biologic. Functional Service Provisi...
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    The tiny-TIMsg system, as part of the SurroGUT™ platform, precisely mimics the upper GI tract and all physiologically relevant processes; including the pressure, shear forces and phase specific gastric emptying. The tiny-TIMsg consists of an advanced gastric compartment (TIMagc) and small intestine co...
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    When you are looking for a partner who is dedicated to Phase I trials and early clinical development, rely on Quotient Sciences for the experience and expertise to seamlessly deliver your studies with the highest quality service and speed. We accelerate your molecule from first-in-human to proof-of-concept...
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    Clinical Development Program (Phase I to IV) Product Registration 
    Pharmacovigilance
    Regulatory Affairs
    Clinical Monitoring 
    Medical Monitoring
    Project Management 
    Medical Writing 
    Quality Assurance - GCP Audits 
    Logistics Coordination 
     
  • Product Biomarker Assays and Validation

    Validation of biomarker assays: Our diverse range of analytical platforms supports biomarker analyses including ELISA, flow cytometry, cell-based assays, multiplex ECL platforms, and high sensitivity measurements using QuanterixSimoa HD-X Analyzer™ measurement instruments. Our dedicated biomarker assay...
  • Product Clinical Supply Solutions Service

    Ardena offers services under brand pharmavize which includes clinical supply solutions service. It has a promising drug molecule and it is preparing for preclinical or early phase clinical studie. Its business is to develop and manage the clinical supply materials, from design to delivery. It bring the api...
  • Product Clinical Trial Conduct & Management

    Prior to the conducting of the clinical trial, the study must be approved by the Research Ethics Committee. Then a Site Initiation Visit (SIV) will be performed and the clinical staff (Medical Doctor, Research Nurses, Clinical Trials Assistant, Nutritionist, Research Technician etc.) will be...
  • Product Bioanaysis

    Delivering rapid bioanalytical data in discovery – preclinical – clinical. Bioanalysis is a critical step in the drug development process.  At Quotient, we are experts in the development, validation, and application of bioanalytical assays.  
    Our dedicated team of bioanalytical chemists...
  • Product Outsourcing

    Patheon by Thermo Fisher Scientific has a broad manufacturing platform for pharmaceutical and biologic products which provides sustainable solutions for mammalian cell-based and microbial-based manufacturing, green chemistry R&D and manufacturing technologies, and finished dosage production of biopharm...
  • 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.

  • Product 2-8°C Clinical Trials, Biologics, Vaccines

    Cold Chain expertise.
    CIT can pack any farmaceutical form at 2-8°C
    Vials, ampoules, bags,...


    Ask for our developed service of 2-8°C monitoring via blockchain
  • Product BDD Swift - adaptive clinical studies

    •SWIFT accelerates evaluation and optimisation of product performance using in vivo clinical data to direct formulation design in real time.
    •SWIFT studies enable you to make decisions on formulation changes based on emerging clinical data. • This integration of formulation development, GMP manufactu...
  • Product Orphan Drug Development

    Accelerating orphan drug development from candidate selection to commercial manufacture and supply.

    With over 300 million people worldwide living with identified rare diseases, the development of new treatments to address these unmet clinical needs is an area of great interest in the pha...
  • Product Clinical Trial Reporting

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    • Developability assessment • Pre-formulation screening • Formulation development • Lyophilization process development • Forced d...
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    Contract Research Laboratory. Analytical Services (physicochemical analysis, microbiological analysis and stability studies) and EU Import Lab.
  • Product Manufacturing Services

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