ABOUT US
GOALS AND MISSION
4Clinics is a Contract Research Organization (CRO) providing Data management, Biostatistics, Scientific Writing, Regulatory Affairs and Clinical Operations services for clinical, observational and epidemiological studies with a particular expertise in vaccines, immunotherapeutics, cell and gene therapies with a dedicated branch for medical devices.
4Clinics provides comprehensive clinical expertise to meet the needs of its clients. It has long experience of clinical trials, allied methodologies and healthcare, and takes pride in giving its clients satisfaction.
4Clinics is member of the Belgian Association of CROs (BeCRO), France Biotech, Biowin (Health Cluster of Wallonia), the French Association of CROs (AFCRO), Medicen (Health Cluster of Paris Region), PHUSE (Non-Profit Organization of Statistical Programmers) and EMWA (European Medical Writers Association)
4Clinics is partner of the French-American Chamber of Commerce, New England | FACCNE
4Clinics benefits from the French Research Tax Credit agreement (“Credit Impôt Recherche”).
MANAGEMENT TEAM
Anne HEPBURN (Ph.D. in Medical Biology) – Senior Advisor – Director Biostatistics
Anne has been Director of Scientific Writing & Regulatory Affairs Services at 4Clinics for more than 15 years. She is a native English speaker and came to 4Clinics with nearly 20 years of experience in clinical research and regulatory affairs. She has extensive experience in preparing clinical trial documentation (protocols, investigator brochures, study reports) and regulatory submissions. She has also written or co-written peer-reviewed articles for pre-clinical and clinical studies.
Christophe GRENOT – Director Clinical Operations & Data Management
Christophe is Clinical Research professional with over 20 years of experience in conducting EU and FDA-regulated trials in a broad range of therapeutic areas. He started his career in hospital before joining the industry and CROs where he led a number of successful clinical projects for start-ups at the forefront of technological advances. Before joining 4CLINICS in 2017, he provided independent consulting services to medical device industries in designing, setting up and following clinical development programs.
Luise KALBE (Ph.D. in Biochemistry) – Director Medical Writing and Regulatory Affairs Services
Luise Kalbe is Head of the Medical Writing and Regulatory Affairs Services Department since
November 2021. She has extensive experience in the pharmaceutical industry, academia, the public
sector, and an NGO. As a medical communications expert, she communicates science to expert and
non-expert audiences in several languages as a medical writer, author of scientific publications, and
lecturer. She is also experienced in publications management, medical affairs, and business
development.
