• In-Vivo

    Bioequivalence/ Bioavailability Studies in Healthy Volunteers (Nontherapeutic Clinical Studies)

  • In-Vitro

    Dissolution and stability studies (pharmaceutical studies)

  • QA services

    Building Quality Systems for science based institutions and CROs



ICBR delivers integrated information and technology solutions for achieving better healthcare.

Pharmaceutical stakeholders trying to provide better healthcare through treatment innovations count on ICBR to provide high quality pharmaceutical and clinical studies. We empower clients to achieve some of their most important goals: Improving clinical, scientific and commercial results.


Services

ICBR - International Center for Bioavailability, Pharmaceutical and Clinical Research


In-Vivo

Bioequivalence/ Bioavailability Studies in Healthy Volunteers (Nontherapeutic Clinical Studies)

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In-Vitro

Dissolution and stability studies (pharmaceutical studies)

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QA services

Building Quality Systems for science based institutions and CROs

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Training services

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  • Well-trained clinical site staff is a key factor in ensuring the success of clinical trials and other health research studies. ICBR's dedicated training professionals and project staff work together to provide support staff with effective and engaging training so that they are equipped with critical knowledge and skills.

  • Training Courses:

    • Protocol writing

    • Good Clinical Practice (GCP)

    • Data Management

    • Analytical procedures

    • Quality Assurance and quality control

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Preclinical studies

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  • Deciding whether a drug is ready for clinical trials (the so-called move from bench to bedside) involves extensive preclinical studies that yield preliminary efficacy, toxicity, pharmacokinetic and safety information. Wide doses of the drug are tested using in vitro (test tube or cell culture) and in vivo (animal) experiments,.

    Much like for clinical trials, there are certain types of trials that have to be done, such as toxicology studies in most cases, Don't get too worked up on too many preclinical trials that may not be necessary but make sure to consult with experts who can help you decide, which trials you should do and if you are ready to move into clinical stage. At Profile we have a team of experts who can advice you on such questions and who will help you with the transition into clinical trials. Contact us to start the discussion.

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REQUEST PROPOSAL

Let us know about your project to get started.

Fill out the brief form below to get in touch

  • Address

    Plot No. 10, Block No. 12018, North Industrial Zone, El-Obour City, Egypt

  • Phone

    +202-4489-1252

  • Email contact

    info@icbr.info

  • Website

    www.icbr-egypt.com