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We are dedicated to promoting speed, excellence and exceptional performance in the advancement of clinical drug development

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EBS provides cost-effective clinical research services to the pharmaceutical and biotech industries

Aiming to bring safe and ethical life-saving products to market by staying up-to-date with industry developments and working closely with clients

QUALITY

We are committed to providing the highest quality services to our clients, ensuring that their products are developed and brought to market safely and efficiently

FLEXIBILITY

We understand that each client’s needs are unique, and we work closely with our clients to tailor our services to meet their specific requirements

INTEGRITY

We strive to maintain the highest ethical standards in all of our operations, ensuring that our clients’ products are developed and brought to market in a responsible and transparent manner

TEAMWORK

We believe that teamwork is essential for success, and we foster a collaborative and supportive environment where all team members can contribute their skills and expertise to achieve our common goals

INNOVATION

We are dedicated to staying at the forefront of the industry, continually seeking new and better ways to serve our clients and improve our services

RESPONSIVENESS

We pride ourselves on our ability to respond quickly and effectively to our clients’ needs, and we are committed to providing timely and accurate information to help our clients make informed decisions

EBS CRO is a leading contract research organization in Serbia that provides a wide range of services to the pharmaceutical and biotech industries

The company is led by experienced professionals who oversee clinical trials, ensure regulatory compliance, provide statistical support, and manage day-to-day operations. EBS CRO also has a team of highly skilled Clinical Research Associates who monitor clinical trial progress. The company is committed to providing high-quality services and has built a strong reputation as a leading local CRO

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EBS CRO was founded in 2010 in Serbia,
after a merger with Acord, which was the first local CRO in the country founded in 2003

The company offers clinical trials, regulatory affairs, and pharmacovigilance services to the pharmaceutical and biotech industries, specializing in regional regulatory requirements. Since its establishment, EBS CRO has become a leading CRO in the region, working with top pharmaceutical and biotech firms

The company provides comprehensive clinical trial-related services and consultancy to pharmaceutical and medical device developers in Serbia and the surrounding Balkans and Southeast Europe region

EBS uses its custom-made software solutions to provide efficient and streamlined services to its clients, while allowing them to retain control of the process. The company is dedicated to working closely with its clients, providing strategic guidance and exceptional service while aligning with their goals and vision. EBS aims to expedite products through clinical trials and bring them to market quickly, making it a valuable partner for clinical trial needs

EBS CRO has established itself as a respected and recognized expert in various indications, including endocrinology, neurology, respiratory disorders, oncology, nephrology, cardiology, infectious diseases, autoimmune disorders, and pediatric studies

The company's scientific approach and extensive local knowledge make it particularly well-suited to successfully conduct complex and difficult-to-recruit clinical trials. EBS CRO provides high-quality, integrated, and customized expertise through its highly standardized management process, innovative product development plans, and effective regulatory strategies. With its ability to deliver studies on time and with high quality, EBS CRO is a valuable partner for clients in the pharmaceutical, biotechnology, and medical device industries seeking to achieve their goals in all phases of clinical product development

PROJECT MANAGEMENT

Our Project Management ensures that all studies are carried out in full accordance with the study protocol, to agreed study timelines, and to other Sponsor-driven parameters

MONITORING

Most Clinical Research Associates working with EBS Clinical Research are MDs and their experience and training ensure the highest clinical research standards

SITE MANAGEMENT

Our approach to Site Management ensures effective patient recruitment with high recruitment rate and reduced time and cost of clinical trials

SITE ASSESMENT

Site selection is the most important step for ensuring both timely recruitment and high-quality study data, therefore we screen and assess sites extensively before including them in studies

FEASIBILITY & STUDY START-UP SERVICES

At EBS CRO, we understand the importance of determining whether your Investigational Medicinal Product is safe and effective to move to the next phase of clinical development or to be marketed

RESCUE STRATEGIES

In case of underperforming studies and poor patient recruitment rate EBS Clinical Research can provide advice on the best choice of centers for rapid study set-up and execution

PHARMACOVIGILANCE

Pharmacovigilance and drug safety complement other services provided by CRO and include services such as identifying, recording and reporting SAEs/SUSARs according to applicable regulations

RECORD MANAGEMENT

Clear document management planning, especially during the critical start-up phase of a project

REGULATORY SERVICES

EBS Clinical Research is able to provide full support for all regulatory and ethics submissions

SAFETY AND MEDICAL MANAGEMENT

Our team of skilled professionals has extensive experience in medical management, pharmacovigilance and the regulatory requirements for safety services