Looking for suitable Contract

Research Organization?

X7 Research company is a contract research organization offering a full range of services at all stages of the development and registration of medicines in Russia, the EAEU, the CIS, and the EU.

send us an email to research@x7cpr.com

Our contract research organization can help in:

  • research and consulting in the process of drug development
  • provide high-quality clinical trials
  • registration, modification of registration dossier etc.
  • post-marketing of the drug
  • organization of the pharmacovigilance system

Our contract research organization provides a systematic approach to solving clinical trials

send us an email to research@x7cpr.com

Do you need more infromation?

    Why clients choose our CRO

    X7 Research company is a contract research organization that provides a full range of services from consulting research, preparation of registration strategy, planning and conducting Phase I-III clinical trials to registration, post-registration studies (Phase IV, NIS) and pharmacovigilance.


    X7 Research’s company primary responsibility is to help our clients in bringing medicines & devices to the market efficiently and safely.

    X7 Research company is ready to conduct clinical trials and provide research support activities

    Our Email: research@x7cpr.com

    Contact us

    WHAT IS Contract Research Organization?

    CROs provide the expert guidance, advice, and execution experience required to complete clinical trials efficiently. So sponsor don’t need to hire personnel on a full time job.
    Within clinical trials, a sponsor (the organization seeking to investigate the safety and effiсiency of a new treatment) hires a CRO to a specific project contract, on a contract, project-by-project basis.
    Services can range from drug discovery to commercialization, pharmacovigilance and post-approval services.
    A contract research organization range of clinical research services to (CRO) provides research services to pharmaceutical, biotechnology, and medical device companies.

    What Does A CROs Do?

    Contract Research Organizations (CROs) — are companies that conduct clinical trials and provide research support services in the field of biotechnology, medical equipment and the pharmaceutical industry, as well as in universities, government organizations and foundations.


    Group 11

    Registration strategy & consulting

    — Data search and analysis

    — Registration strategy development

    — Study feasibility

    — Vendor selection

    — Budgeting

    X7 Research company has extensive experience in finding and analyzing information about specific medicines to prepare a drug registration strategy in Russia, the EAEU, the CIS, the EU.

    Post-authorization clinical studies

    — Phase IV studies

    — Non-interventional studies

    — Post-authorization safety

    X7 Research company offers a wide range of services in the post-marketing phase of the drug lifecycle. Our company are ready to conduct both large-scale studies to obtain big amounts of real-world data (RWD) and small-scale exploratory studies. The X7 Research company team is ready for any challenge and the most ambitious projects.

    Group 15


    — Phase IV studies

    — Non-interventional studies

    — Post-authorization safety 

    X7 Research company offers a wide range of services in all phases of building a pharmacovigilance system, from individual consultations to complete pharmacovigilance.

    Clinical trials

    — Development of medical documentation and biostatistics

    — Monitoring

    — Data management

    — Patient home visit

    — Bioequivalence study

    — Therapeutic equivalence studies

    X7 Research team are always trying to find individual solutions for each clinical trial and each partner.


    —  Audit of the registration dossier

    — Bringing the registration dossier in compliance with the requirements

    — Conversion of registration dossier into XML format

    — Custom testing of the package insert

    X7 Research company provides services for state registration, modification of registration dossier, confirmation of state Registration of domestic, foreign, original, and reproduced medicines on the territory of the Russian Federation and the Eurasian Economic Union countries.


    Our email: research@x7cpr.com

    Our goal is to conduct research activities, explore the potential of young professionals and expand the development prospects of both employees and the pharmaceutical industry

    Contract Research Organization Roles and Responsibilities

    A CRO is responsible for planning, setup, and day-to-day execution, management of a clinical trial. Handling and supervising the technical — data collection and medical testing aspect.

    Clinical compliance with regulatory agency guidelines is crucial, and adhering to Good Clinical Practice (GCP) standards. CROs role as the trial’s central hub connecting the sponsor with other stakeholders such as regulatory agencies, ethics committees, vendors, hospitals, etc.



    We help organizations trade with integrity and trust


    We ensure safety in everyday life, at home and at work


    We help new technology to reach consumers quickly

    Do you ready to choose X7 Research company as a CRO? Email us to research@x7cpr.com


      Outsourcing to a Contract Research Organization can bring multiple benefits to clinical professionals and institutions.

      Time Savings

      Working with a CRO to conduct a trial often significantly reduces the time it takes compared to completing the trial in-house.

      CROs have already had all necessary tools and resources as well as a team experts who are experienced in all areas of clinical testing, development, and compliance.

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