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 the EU,
the EAEU, the CIS, and in Russia.
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
send us an email toresearch@x7cpr.com
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.
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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
Contact us Our Email:
research@x7cpr.com
WHAT IS Contract Research Organization?
A contract research organization range of clinical research services to (CRO) provides research services to pharmaceutical, biotechnology, and medical device companies.
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.
OUR SERVICES
– 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.
– 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.
– 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 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
OUR PURPOSE
Better
We help organizations trade with integrity and trust
Safer
We ensure safety in everyday life, at home and at work
Interconnected
We help new technology to reach consumers quickly
Outsourcing to a Contract Research Organization can bring multiple benefits to clinical professionals and institutions.
Time Savings
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.
Trials Cost Savings
There are significant cost savings in hiring a CRO. A faster trial process alone offers medical institutions a reduction in costs.
You don’t need to hire personnel, especially when they are not needed during the year.
Advanced Technological Needs
Clinical research is a rapidly changing industry. It is essential that software and hardware IT capabilities, as well as Internet-based applications, are the best in the industry to facilitate the acceleration of clinical trials while maintaining comprehensive quality control.
Evolving and Complex Regulatory Requirements
The FDA and other relevant regulatory authorities require intricate and accurate data for approvals. CROs work within clinical compliance on a daily basis, which gives them intricate knowledge of regulatory requirements and audits such as Good Clinical Practice (GCP) audits or Good Laboratory Practice (GLP) audits.
CROs work with hiring companies to optimize audit results through careful review of any previous issues, close inspection of infrastructure, and adherence to current protocols.
13
years of experience
25
projects involved
90%
of international clients
55
open sites
This is what our clients say about us:
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What is a contract research organization in Clinical Trials?
How X7 RESEARCH company works
Conducting a gap analysis
Literature review
Document review
Preparing a drug
Working with a CRO
There is 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 niche area.
Comparing one CRO to another can be very difficult, as CRO budgets and services often vary significantly from one company to the next. When selecting a CRO, take into account 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.
When hiring a CRO, always ensure each delegated task is outlined in writing and signed by both parties. All agreements should be thoroughly documented by all of the involved parties to avoid any costly misunderstandings or complications.
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.
The quality and integrity of the 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.
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 clinical research and manufacturing work continues to develop as organizations aim to meet the needs of an evolving industry.
START A PROJECT WITH X7 RESEARCH
send us an email to research@x7cpr.com
NEWS
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FAQ
What is a Contract Research Organization?
Is CRO the same as Contract Research Organization?
In what countries does X7 Research company operate?
What is a Clinical Research Organization?
Does X7 Research company have a standard quality certification?
What services does X7 Research company provide?
What is a Clinical Research Partner?
