DEDICATED EXPERTS TO ASSIST YOU
IN THE DEVELOPMENT OF YOUR PROJECT

SERVICES

From the early conception to the post-marketing studies of the drug, CARES provides you with a complete panel of assessment and consultancy services and tools. We are here to offer our expertise in the field and help your project take shape and arise successfully in the best circumstances.

Consultancy

CARES gathers a range of experts to assist you in the development of your project, from the early conception to the post-marketing studies. Our consultancy services are broad and varied:

Help in the development of the molecule
Scientific literature and documentation study
Assistance in the EMA (European Medicines Agency) Authorization process
Support in the launch of your product

We are happy to put all our skills and experience at work for every stage of the project life cycle and help you concretize your creation.

QUALITY ASSURANCE

Through a strategic partnership with CHU of Liège, CARES ensures the provision of high-quality services, guaranteeing that results comply with the strictest quality assurance standards. This partnership combines advanced clinical expertise and multidisciplinarity with rigorous process quality control.

Laboratory of CHU of Liège holds various accreditations and certifications, which ensure the reliability of results and the handling of samples, including:

BELAC Accreditation

Accreditation by BELAC, the Belgian national accreditation body, confirms that analyses are conducted in accordance with the strictest international standards of quality and technical competence. This accreditation includes two certifications:

- BELAC 128 MED (ISO 15189): This certification defines the quality and competence require- ments specific to medical laboratories, ensuring precise and reliable diagnostic results.

Sciensano

In partnership with Sciensano, the Belgian scientific institute for public health, rigorous protocols based on the latest scientific research are applied to ensure the reliability of results.

GCP (Good Clinical Practice) Standards

Clinical research is conducted in compliance with Good Clinical Practice (GCP), an internation- al standard that guarantees ethics and quality in clinical trials involving human participants.

GLP (Good Laboratory Practice) Standards

Laboratory activities adhere to Good Laboratory Practice (GLP), ensuring the quality and rigor of non-clinical studies through standardized and documented processes.