Looking for suitable Contract Research Organization?

Looking for suitable Contract

Research Organization?

X7 Research company is a contract research organization (CRO) offering a full range of services at all stages of the development and registration of medicines, biostatistical consulting in Russia, the EAEU, the CIS, and the EU. X7 Research have offered a reliable partnership for pharmaceutical, biotechnological enterprises since 2010.

send us an email to info@x7research.ru

Our contract research organization can help in:

  • research and consulting in the process of clinical trials 
  • providing clinical trials for your medical devices and drugs
  • registration of drug and medical devices according to regulators 
  • we offer a wide range of services in the post-marketing phase of the drug lifecycle
  • well qualified organization of the pharmacovigilance system
  • home care service for patients
  • biostatistical consulting for your clinical trial

X7 Research conducts research activities, exploring the potential of young professionals and expanding the development prospects of both employees and the pharma industry.

send us an email to info@x7research.ru

Do you need more infromation?

    send us an email to info@x7research.ru

    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 registration, biostatistical consulting and pharmacovigilance. Our clients are local companies as well as Big Pharma. Our clients stay with us and conduct several clinical trials in a row.


    X7 Research’s primary responsibility is to help our clients to bring medicines and devices to the pharmaceutical market efficiently and safely, as quickly as possible and within your budget. 

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

    Contact us

    Our Email: info@x7research.ru

    WHAT IS Contract Research Organization?

    CROs provide the expert guidance, advice, and execution experience required to complete clinical trials efficiently. Using the services of a contract research organization, the sponsor does not need to hire a full-time CTA and other employees, because the CROs can provide its own staff.
    Sponsor an organization that needs to conduct clinical trials within the current legislation. For many companies, it is more profitable and convenient to purchase CRO services for a specific project contract, on a contract basis, project by project. 
    Services may vary depending on the therapeutic area, kind of a drug or a medical device, what is specifically required when conducting research in the pharma industry.
    A contract research organization (CRO) provides a range of clinical research services conducts clinical trials of early, late and biostatistical phases, biostatistical consulting and offers pharmacovigilance services, registration, and many others depending on the specifics of this CRO.

    What Does A CROs Do?

    Contract Research Organizations (CROs) are companies that conduct clinical trials and provide research support services in the fields of biotechnology, medical devices, and the pharma industry, focusing on conducting research within the established budget, respecting research deadlines.


    Group 11

    Registration strategy & consulting

    Registration strategy & consulting

    – Research and analysis data

    – Development of a strategy for the registration of drugs and medical devices in the pharma

    – Study feasibility of clinical trials

    – Choosing a vendor according to your research

    – Budgeting in advance of any clinical trial for better study design

    X7 Research has extensive experience in searching and analyzing information on specific medicines in various therapeutic areas in order to prepare a strategy for registering medicines under the laws of Russia, the EAEU, the CIS, the EU. Scientific department of X7 Research performs qualitative and quantitative evaluation of sources to prepare completed documents in any therapeutic area and in the biostatistical consulting.

    Post-authorization clinical studies

    – Phase IV studies

    – Non-interventional studies

    – Post-authorization safety

    – biostatistical consulting

    X7 Research offers a full range of services for the post-marketing stage of the drug life cycle. Our company is ready to conduct both large-scale studies to obtain large volumes of real data (RWD) and small-scale exploratory studies. Biostatistical consulting is also an essential aspect of any clinical trial. The X7 Research team is ready for any challenge and the most ambitious projects. We are always trying to find individual decisions to each project. 

    Group 15


    – Building a system of pharmacovigilance

    – Safety in clinical trials

    – Pharmacovigilance audit

    – Pharmacovigilance contact person

    – QPPV in FV system 

    Pharmacovigilance remains one of the most important parts of conducting a clinical trial. That is why our CRO offer a full range of pharmacovigilance services.

    Clinical trials

    – Development of medical documentation and biostatistics

    – Monitoring your clinical research

    – Data management

    – Patient home visit 

    – Bioequivalence study

    – Therapeutic equivalence studies

    Our CRAs are verifying that subjects’ rights and welfare are protected, the data submitted is accurate, complete, and supported by primary documentation and the study is conducted by the approved current version of the protocol/amendments, GCP, and regulatory requirements


    –  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 a registration dossier, confirmation of state registration of domestic, foreign, original, and reproduced medicines in the territory of the Russian Federation and the Eurasian Economic Union countries.


    Our email: info@x7research.ru

    Our goal is to continually research, improve and conduct quality clinical research in accordance with your therapeutic area, the length of your clinical trial and your budget. X7 Research is a reliable partner for the trials in challenging regulatory environment and tough economy.

    Contract research organization roles and responsibilities in pharma

    A CRO is responsible for the planning, setup, and day-to-day execution and management of a clinical trial and they offer a lot of services, for example, biostatistical consulting. An important task of the CRO is also supervision and monitoring, check the correctness of filling out reporting documents and the technical aspects of the study. 

    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.


    X7 Research’s company primary responsibility is to help our clients in bringing medicines & devices to the market efficiently and safely. We are a reliable partner in clinical trials since 2010. We are highly experienced in conducting clinical trials, providing market analysis, conduct biostatistical consulting and so on.


    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 info@x7research.ru


      Outsourcing to a Contract Research Organization can bring multiple benefits to pharma companies.

      Time Savings

      Working with a CRO to conduct a clinical trial often significantly reduces the time required compared to completing a trial in-house, as the CRO has expertise in record keeping, routine testing, and a faster process for writing key documents: investigator brochure, trial protocol, and others.

      CROs have already had all the necessary tools and resources, as well as a team of qualified experts with experience in all therapeutic areas of clinical trials, development, compliance and biostatistical consulting services.

      Trials Cost Savings

      When a sponsor uses the services of a CRO, significant savings can be made on the outsourcing of pharmacy personnel. By itself, a faster litigation offers healthcare providers cost savings

      X7 Research offers staff outsourcing for your specific clinical trial, allowing you to reduce staffing costs in the pharma industry

      Advanced Technological Needs

      Working with CRO provides hiring companies with access to the most advanced technologies and systems for data management, product development, research analysis and other clinical research services in any field of pharmacy.

      Clinical trials industry  is a rapidly changing that requires advanced IT solutions, computer-assisted data management, and validated record keeping technologies.

      Evolving and Complex Regulatory Requirements

      Regulatory authorities require complex and precision information from sponsors to validate and control the quality of pharmaceutical clinical trials. CROs work within a clinical compliance framework on a daily basis, which gives them detailed knowledge of regulatory requirements and audits such as Good Clinical Practice (GCP) audits.

      CROs work with hiring organizations to optimize audit results through careful review of any previous issues, close inspection of infrastructure, and adherence to current protocols.

      Let’s check some X7 Research figures


      years of experience


      projects involved

      more than


       of international clients


      open sites

      Our company works with you from the first stages of clinical trial to the final registration the drug

      Our Email: info@x7research.ru

      This is what our clients say about us:

      What is a contract research organization in Clinical Trials?

      What is a contract research organization in Clinical Trials?

      The CRO is a contract research organization that plans, develops, and coordinates the validity of  conducting a clinical trial processes according to a trial protocol. It then performs this protocol in accordance with the rules of the regulatory body and GCP standards. Also, an integral part of the work of the СRO is the work with the principal investigators of the sites and with patients.

      A sponsor — who might have many potential treatments they wish to have tested via clinical trial — engages a contract research organization to take care of the time-consuming and resource-intensive work required of a clinical trial or biostatistical consulting. The sponsor is able to leverage the expertise of the CRO, which due to the CRO’s repeated execution of trial after trial, comes to be able to anticipate potential delays and pitfalls, avoiding them ahead of time.

      How X7 RESEARCH company works


      Conducting a gap analysis


      Literature review


      Document review


      Preparing a drug registration strategy

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

      Do you need more infromation?

        send us an email to info@x7research.ru

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

        send us an email to info@x7research.ru

        Working with a CRO
        Group 17 (1)

        Selecting a CRO

        There are a wide variety in CROs. Some are large, publicly owned companies with global coverage and a range of comprehensive services, while other CROs are small, privately owned companies that specialize in a specific area.

        Comparing one CRO to another can be very difficult, as CRO budgets and services often vary significantly from one company to another. When choosing a CRO, look at the company’s previous experience, including the types of projects completed, the clients they have worked with, any niche services they provide, as well as their overall track record in the industry. For example, there are a lot of biostatistical consulting firms and biostatistical consulting company. Also, an important part of the work of a contract research organization is work in various therapeutic areas: cardiology, oncology, ophthalmology, neurology, and many other areas.

        Sponsor’s Responsibility

        A business, organization, or institution may outsource any or all its clinical trials and research responsibilities to a Contract Research Organization, but the responsibility remains with the original company that hired the CRO. Therefore, the sponsor is responsible for the safety of the investigational product in clinical trials.

        The quality and integrity of a  clinical research data continue to reside with the entity sponsoring the work. CROs should be backed by a spotless track record of quality assurance and quality control to be competitive with other organizations.

        Get It In Writing

        A clinical research is very expensive, it should be clear which organization are responsible for each aspect of medical research, development, biostatistical consulting services or other clinical services. Responsibility for any services or components not specified in the agreement remains with the sponsor, that is, the organization employing the CRO.

        It should be very clear which organization is responsible for each aspect of the medical research, development, or other clinical services. Any services or components that are not specified in the agreement will remain the responsibility of the hiring entity.

        What Is CRA and Manufacturing Services?

        Contract Research and Manufacturing Services (CRAMS) is a broader clinical outsourcing term that includes CROs as well as CMOs, Contract Manufacturing Organizations.
        Contract Manufacturing Organizations (CMOs) are similar to CROs, in that they are also hired by another pharmaceutical company on a contract basis. The purview of a CMO is in the development of a drug through to its manufacturing.

        They all make up a rapidly expanding segment of the biotechnological and pharmaceutical industry. Outsourcing specialized in clinical research and manufacturing work continues to develop as organizations aim to meet the needs of an evolving industry.


        send us an email to info@x7research.ru


        It’s important to respond quickly to an ever-changing environment in a COVID-19 pandemic.  Today we will tell you how to function with clinical trials in accordance to new conditions. 

        Market share of original medicines in Russia is incredibly small because of great costs of drug development, pre-clinical and clinical trials of an original drug.

        Russian pharmaceutical market size in 2016 reached 1,344 billion rubles, which is 7% higher than a year earlier, and in 2017 reached 1,629 billion rubles, which is 8% higher than in 2016.


        What is a Contract Research Organization?

        A contract research organization (CRO) is a company that provides support to the pharmaceutical, biotechnology, and medical device industries by offering research services on a contract basis. A contract research organization may provide such services as biopharmaceutical development, biologic assay development, commercialization, preclinical research, clinical research, contract research, clinical trials management, and pharmacovigilance

        Is CRO the same as Contract Research Organization?

        CRO is the abbreviated form for Contract Research Organization

        In what countries does X7 Research company operate?

        X7 Research company is a Contract Research Organization offering a full range of services at all stages of drug development and registration in Russia, EAEU, CIS, and EU

        What is a Clinical Research Organization?

        X7 Clinical Research is a modern center specializing in conducting clinical studies in bioequivalence and Phase I, II, III studies and post marketing drug research. Clinical center is equipped with modern equipment and has a well-developed infrastructure, including all the necessary premises for conducting clinical trial. In addition, company has an extensive referral network of doctors to invite patients and healthy volunteers.

        Were there audits in X7 Research company?

        X7 Research had frequency audits from Big pharma. We are qualified vendor for more than 100 pharma companies.

        What services does X7 Research company provide?

        X7 Research company offers services «in house» in the area of clinical research, bringing outsourcing solutions to the Pharmaceutical, Drug, Biological and Device Industry. Design of study documents, selection and management of investigational sites, subject recruitment, project management and monitoring.

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