Looking for suitable Contract Research Organization?
Looking for suitable Contract
X7 Research is a reliable partner in clinical trials, registration drugs and medical deviсes, pharmacovigilance consulting, a wide range of services in a post-marketing phase of the drug lifecycle since 2010. Our company is a contract research organization (CRO) proposing a full range of research services at all stages of the development and registration of medicines and devices in Russia, the EAEU, the CIS and the EU.
Our contract research organization can help in:
- research and consulting in the process of drug development
- conducting high-quality clinical trials phase I-IV
- registration of drugs, assistance in compiling and changing the registration dossier
- post-marketing of the drug
- organization of a pharmacovigilance consulting, maintaining documentation within the legislation
- nursing service
Our contract research organization (CRO) provides a systematic approach to solving clinical trials and pharmacovigilance consulting
Why clients choose our CRO
X7 Research is a contract research organization (CRO) with a large team of highly qualified specialists providing a full range of services from consulting, research, preparation of a registration strategy, planning and conducting pre-registration phases I-III clinical trials, medical writing, post-registration research (Phase IV, NIS) and pharmacovigilance consulting. We offer a full range of services that is our main advantage.
X7 Research’s company primary responsibility is to help our clients in bringing medicines & devices to the market efficiently and safely.
WHAT IS Contract Research Organization?
What Does A CROs Do?
Contract Research Organizations (CROs) are the companies that conduct clinical trials for a sponsor and provide research support services to pharmaceutical, biotechnological and other organizations with different services. For example, pharmacovigilance consulting companies offer their services in the field of monitoring for drugs after clinical trials and so on
Registration strategy & consulting
– Data search and analysis
– Registration strategy development
– Study feasibility
– Vendor selection
– Consulting services
X7 Research has extensive experience in searching and analyzing information on specific medicines to prepare a strategy for the registration of medicines and medical devices in Russia, the EAEU, the CIS, the EU.
Post-authorization clinical studies
– Phase IV studies
– Non-interventional studies
– Post-authorization safety
– Consulting services
X7 Research offers a wide range of services in the post-marketing phase of the drug lifecycle. X7 Research is ready to conduct both large-scale studies to obtain big amounts of a real-world data (RWD) and small-scale exploratory studies. A post-marketing research should also be carried out in accordance with applicable law. The X7 Research team is ready for any challenge and the most ambitious projects.
– Building a system of pharmacovigilance
– Safety in clinical trials and in pharmacovigilance
– A Pharmacovigilance audit
– A Pharmacovigilance contact person
– Pharmacovigilance consulting
– Another pharmacovigilance services
X7 Research company offers a wide range of services in all phases of building a pharmacovigilance system. With a great experience in pharmacovigilance, X7 Research offers a full range of FV services in the EAEU that enable you to meet pharmacovigilance requirements of the market. Our pharmacovigilance specialists carry out high-quality documentation of PSUR, DSUR and other services. We grow up every day to our clients for drug consulting formation pharmacovigilance.
– Development of medical documentation and biostatistics
– Outsoursing CRAs
– Data management services
– Patient home visit
– Consulting for clinical trials
– Bioequivalence study
– Therapeutic equivalence studies
X7 Research team is always trying to find individual solutions for each clinical trial and each partner. Our partners note good CRAs work in terms of conducting visits to research centers, as well as the high qualification of our specialists.
– Audit of the registration dossier
– Bringing the registration dossier in compliance with the requirements
– Conversion of the registration dossier into XML format
– Custom testing of the package insert
– Registration consulting
X7 Research provides services for a state registration, modification of the registration dossier, confirmation of a state registration of domestic, foreign, original, and reproduced medicines on the territory of the Russian Federation and the Eurasian Economic Union countries. The area of interest of our company: to work with the registration of medical devices according to the rules of the EAEU. Now this is relevant for certain medical devices of class 2b, 3 and implanted staff.
START A PROJECT WITH X7 RESEARCH
Our goal is to conduct research activities, provide quality services for partners in the field of clinical trials, pharmacovigilance consulting and registration of medicines and medical devices. Our priority is the development of the pharmaceutical field and young professionals.
Contract Research Organization Roles and Responsibilities
The CRO is responsible for a planning, a routine execution, and a management and design of a clinical trial. An important part is the processing of information during the study, a review of the technical aspects of a data collection and medical testing and pharmacovigilance consulting. Clinical compliance is critical, as is adherence to Good Clinical Practice (GCP) standards.
There are a lot of different CROs that responsible for various aspects of clinical trials. For example, pharmacovigilance consulting firms responsible for pharmacovigilance documentation, registration services allow CROs to be more flexible and responsible for registrations consulting.
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
X7 Research’s primary responsibility is to help our clients to bring medicines and medical devices to the market efficiently and safely according to our pharmacovigilance system. We help clients to work within tight budgets and deadlines. We have been a reliable partner in clinical trials since 2010.
BENEFITS OF OUTSOURCING TO A CRO
Outsourcing to a Contract Research Organization (CRO) can bring multiple benefits to clients in pharma in clinical trials and pharmacovigilance.
Working with a CRO to conduct research is reduced time required compared to completing the test in-house. CRO has already had all the necessary tools and resources, the team of professionals in the field of clinical research in various therapeutic areas.
The accumulated experience in our company, the system of SOPs and an individual approach significantly reduces the time for conducting research. Sponsor doesn’t need person in his staff for pharmacovigilance consulting because we have already had PV.
Trials Cost Savings
The team in the contract research company (CRO) is already formed, so you do not need to hire additional staff for clinical research for your clinical trials.
You don’t need to spend a lot of money for staff and consulting services and pharmacovigilance persons.
Working with CRO gives hiring companies access to the most advanced technologies and systems for a data management, a product development, research analysis, innovative IT-technology solutions, good pharmacovigilance system and other clinical research services.
Keeping up with the times is especially important in the fast-growing pharmaceutical industry.
Evolving and Complex Regulatory Requirements
Current legislation is constantly changing in pharmacovigilance especially, that is why the competence of contract research organizations (CROs) includes constant local expertise. It is very important to follow Good Clinical Practice (GCP) to provide quality services to partners and clients.
Therefore, sponsor audits are often carried out for organizations, which X7 Research always passes.
Let’s check some X7 Research figures
years of experience
of international clients
Our company works with you from the first stages of clinical trial to the final registration the drug
This is what our clients say about us:
What is a contract research organization in Clinical Trials?
During our partnership, we have jointly completed over 10 projects. The projects covered a variety of tasks, such as writing of medical documentation, conducting all types of monitoring visits, preparation of a final clinical trial report. All tasks were accomplished in time, the patient enrollment at the site followed the schedule, and the work provided was at a high-quality level.
In the course of our partnership, we valued the high level of provided services, responsibility, and professionalism of the team. During the collaboration period, X7 Research was proven to be a responsible and trustworthy partner.
What is a contract research organization in Clinical Trials?
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 consulting services.
The sponsor, who may have many potential treatments that they would like to test in clinical trials, hires a contract research organization. It is necessary to perform time-consuming and resource-intensive work for a clinical trial, for example, for pharmacovigilance documentations. The sponsor may use the experience of the CRO, which, due to repeated CRO testing.
How X7 RESEARCH company works
Conducting a gap analysis
Preparing a drug registration strategy
Selecting a CRO
There is a variety of contract research organizations (CROs) depending on the specialization of companies, its scale, the number of current projects, for example, companies’ formation pharmacovigilance drug consulting.
When choosing an organization for a project, always pay attention not only to the cost of services, but also to previous experience. Also, an important part is the specialization and therapeutic area of this СRO.
A business, organization, or institution may transfer any or all of their clinical trials and research responsibilities over to a Contract Research Organization, but the responsibility remains with the original company hiring the CRO. The quality and integrity of the clinical research data continue to reside with the entity of the sponsor
CROs should be backed by a spotless track record of quality assurance and quality control for pharmacovigilance consulting, for the quality of clinical trials, for registration process.
Get It In Writing
When hiring a CRO, always make sure that each delegated task is in writing and signed by both parties. This will avoid misunderstandings during the clinical trial. Responsibility for any services or components not specified in the agreement remains with the hiring organization. Therefore, contract research organizations (CROs) should provide quality services to the sponsor to not undermine reputation.
For example, it is very important to correctly fill out pharmacovigilance consulting documentation and do it according to deadlines.
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 the CMO is in the development of a drug through to its manufacturing.
All of them make up a fast-growing segment of the pharmaceutical industry. Outsourcing of specialized clinical research and pharmacovigilance persons and manufacturing activities continues to grow in all countries as organizations strive to meet the needs of an evolving industry.
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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.
A contract research organization (CRO) is a company that provides support to the pharmaceutical, biotechnology, and medical devices industries by offering research services on a contract basis. A contract research organization may provide such services as biopharmaceutical development, biological assay development, commercialization, preclinical research, clinical research, contract research, clinical trials management, and pharmacovigilance consulting
CRO is the abbreviated form of Contract Research Organization.
X7 Research company is a Contract Research Organization offers a full range of services at all stages of drug development and registration in Russia, EAEU, CIS, and EU
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 trials. In addition, company has an extensive referral network of doctors to invite patients and healthy volunteers and strong pharmacovigilance system.
X7 Research had frequent audits from Big Pharma. We are qualified vendor for more than 100 pharma companies.
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, monitoring and pharmacovigilance consulting.
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