Contract research organizations (CROs), also known as clinical research organizations, provide a wide range of technical expertise and development support.
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Such organizations are also used by those involved in pharmaceutical, biotechnology, as well as many medical device companies, often on a contractual basis.
Providing outsourced pharmaceutical and biotechnology research services, top contract research organizations help move therapies from concept to market.
This is all done while ensuring full and ongoing compliance with rigorously monitored national and international standards.
Leading contract research organizations and companies
Our Clinical Trials Arena team has researched and listed some of the leading contract research organizations.
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Having compiled this based on its experience in the sector, the team also looked at the various companies that are currently leading the industry.
Included within this content is a list of leading providers of services and products relevant to this sector.
These include:
-Customised services for the clinical development of new drug substances and drug products
-Biotechnology research, preclinical services
-Clinical research services
-Clinical endpoints adjudication management software for clinical trials
-Clinical data analysis, and modelling, research, and development services for clinical studies and regulatory affairs
-Quality control testing, and mass spectrometry services for material characterisation.
Our content also explores a range of suppliers of cell-based in-vitro models, cell-based assay kits, disease models, biomarkers, and recombinant proteins and formulation.
Our download is of particular value to pharmaceutical executives, research scientists, associates, clinical trial managers, specialists, suppliers, and others involved in contract research organizations and associated operations in the sector.
Also contained within this content is some detailed information on the manufacturers and suppliers and their product and service offerings, along with contact details where available.
Industry leading services and systems offered by clinical research organizations
Within the healthcare industry, CROs offer a range of services for various stages of product development, clinical trial, review and marketing.
Some of the current industry leading services include, without necessarily being limited to:
- Formulation expertise in the research and development stage
- Preclinical and clinical studies stage: site selection, patient recruitment, efficacy and safety profiling, database design and implementation, data management, statistical analysis, assessment, validation, and reporting
- Application and review stage: report submission and correspondence support
- Post-approval stage: marketing assistance and post-market safety monitoring
CROs reduce the sponsors’ workload and support the companies in bringing their products to market on time in a cost-efficient manner, avoiding the company’s need to establish in-house facilities for all the research and clinical trial processes.
They may also provide innovative technological tools to companies for more efficient clinical trial processes.
FAQs
What services do Contract Research Organizations provide?
CROs offer comprehensive research services, supporting the entire lifecycle of clinical trials.
Their services include preclinical research, clinical trial management, regulatory submissions, data management, and statistical analysis. They also assist with patient recruitment, site selection, and post-market safety monitoring, helping sponsors develop and commercialise new therapies.
How do CROs help with clinical trial efficiency?
CROs improve efficiency by streamlining trial processes, reducing timelines, and managing regulatory complexities.
They offer expertise in trial design, site coordination, and real-time data monitoring, allowing sponsors to focus on core research while ensuring trials run smoothly and meet deadlines.
What role do CROs play in regulatory compliance?
CROs handle the complex regulatory landscape by ensuring that clinical trials comply with local and international laws.
They manage documentation, ethics committee approvals, and regulatory submissions, minimising the risk of non-compliance and expediting the approval process.
How do CROs support patient recruitment for clinical trials?
CROs have dedicated teams that specialise in patient recruitment strategies, including outreach, eligibility screening, and retention.
They leverage data-driven methods, patient registries, and digital platforms to identify suitable participants, ensuring trials meet enrolment targets efficiently.
What are the advantages of outsourcing clinical trials to a CRO?
Outsourcing to a CRO reduces the sponsor’s operational burden, providing access to experienced teams, cutting-edge technologies, and global trial networks.
This helps pharmaceutical companies avoid the need to build in-house infrastructure, leading to cost savings, faster trial execution, and improved access to global markets.
