Who we are

AdClin is a CRO specializing in clinical data management. Founded in 1999, the company quickly established itself as a key player in the application of CDISC (Clinical Data Interchange Standards Consortium) standards, thanks to its technical expertise and rigorous approach.

We are particularly recognized for our commercialized tools, our mastery of SDTM and ADaM standards, and we assist our clients in the processing, analysis, and submission of clinical data while adhering to the highest standards of quality and compliance.

Our Expertise

CDISC Standards Specialists : For over 25 years, we have been putting our expertise to work for our clients, with a team of professionals who have between 7 and 25 years of experience with these standards.

Training and Knowledge Sharing : We have trained over 200 professionals in SDTM and ADaM standards, and we regularly participate in conferences (CDISC Interchange, GUF CDISC) to share our expertise.

Controlled Terminology : As specialists in Controlled Terminology, we closely follow each update to the terminologies, ensuring that our projects are always aligned with the latest developments.

Our team

AdClin is primarily a team of passionate and committed experts, with backgrounds ranging from Master's (Bac+5) to PhD (Bac+8). Each of our team members is versatile and capable of managing all aspects of a project, whether in SDTM, ADaM, or TFL (Tables, Figures, Listings). This collective expertise allows us to meet the specific needs of each client while ensuring maximum flexibility in resource allocation.

Our presentations

What is the Use of the Controlled Terminology ? An overview of the rules for using controlled terminology

Le « b-a-ba » du standard ADaM, mise en pratique An overview of ADaM standard documents

Retour d'expérience sur la vérification de package CDISC pour soumission à la FDA. Some key points to improve the quality of a submission package