Stemming from the merger of two reference CROs in pharmacology and toxicology (CERB and RTC), European Research Biology Center (ERBC) is a European leader in non-clinical studies. 
It offers to healthcare and chemical professionals a comprehensive range of experimental capabilities, preclinical models, regulatory pre-IND package and consultancy services to de-risk innovation and improve R&D productivity.

Based in Baugy (France) and Roma (Italy), ERBC provides all services from preclinical proof-of-concept to market of any type of drug candidate or chemical compound. Each project is managed by a study director, relying on a multi-disciplinary team of experts, notably in general pharmacology, cardiology, electrophysiology and pathophysiology, also benefiting from a world class academic and private network.

Every year, study reports from our two Centers are successfully used in support of market authorization and new product approval submissions around the world, including the European (EMA, ECHA), US (FDA and EPA) and Japanese (MHLW and MAFF) regulatory authorities.

Investment in outstanding scientific and technical manpower, high-tech equipment and facilities are crucial cornerstones of our sound and organic growth. The quality and reliability of our performance is reflected by the many ongoing and long-lasting collaborations we maintain with leading international pharmaceutical and chemical companies.

ERBC is deeply engaged in animal ethics and welfare. ERBC supports the Basel Declaration, respects the 3Rs concept and continually improves its tools and procedures to maximize the balance between the benefit for health and the animal well-being.

Life Sciences

Pharmaceutical

ERBC (European Research Biology Center)

ERBC (European Research Biology Center)'s headquarters in Baugy, France

This department focuses on advancing scientific knowledge through innovative research and development in medical imaging and in vitro techniques.

Research and Development

The Business Development team at ERBC is responsible for identifying and securing new business opportunities, forming strategic partnerships, and expanding the company's market presence in the healthcare and chemical sectors. They work closely with potential and existing clients to understand their needs, promote ERBC's comprehensive range of non-clinical research services, and tailor solutions that facilitate successful project outcomes. This team plays a key role in driving revenue growth and enhancing ERBC's reputation as a leader in preclinical studies.

Business Development

This department oversees the planning, execution, and oversight of various studies and research projects.

Study Management

The Scientific Team at ERBC is responsible for designing, conducting, and overseeing a range of non-clinical studies to support the development and market approval of drug candidates and chemical compounds. They ensure scientific rigor in experimental setups, interpret data, and compile comprehensive study reports for regulatory submissions worldwide. Additionally, the team consults with clients to de-risk innovation and enhance R&D productivity, while adhering to high standards of animal ethics and welfare.

Scientific Team

This department oversees and conducts research and studies related to toxicology, including the evaluation of chemical substances and their effects on health and the environment.

Toxicology Department

The Quality Assurance Team at ERBC ensures the accuracy, reliability, and compliance of all non-clinical studies and regulatory submissions. They conduct thorough audits, implement standardized protocols, and manage documentation to uphold the highest standards of quality and ethical integrity. This team also ensures adherence to regulatory requirements set by authorities like EMA, FDA, and MHLW, thereby supporting the successful market authorization of new products.

Quality Assurance Team

The Leadership Team at ERBC comprises the CEO, Chief Officer of Global Quality & Compliance, Chief Commercial Officer, and Chief Scientific Officer. This team's primary responsibilities include setting strategic direction, ensuring regulatory compliance, driving commercial growth, and overseeing scientific innovation. They work together to align the company's goals with industry standards and ethical principles, fostering a culture of excellence and accountability.

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Other teams

Business Development

Study Management

Scientific Team

Toxicology Department

Quality Assurance Team

Leadership Team