Generis MEDDRA Integration
CARA Life Sciences Safety Logo copy.png

MedDRA Integration

MedDRA Integration


Ensure the data in your CARA Life Science Platform meets the standards and norms of the MedDRA dictionary / thesaurus

What is MedDRA?

A subscription-based product of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH)

Why is it used?

Provides a rich and highly specific standardised medical terminology to facilitate sharing of regulatory information internationally for medical products used by humans

How will we use it?

By integrating the CARA platform with governed and regulated dictionaries from MedDRA, CARA LifeScience products will provide internationally standardised terms in the regulated industry. These terms would be used in registration, documentation and safety monitoring of medical products both before and after a product has been authorised for sale. This includes all applications in pharmaceuticals, biologics, vaccines and drug-device combination products


minute read

Generis Partners with Christian Schmitz-Moormann to expand PV Capabilities on the CARA LS Platform


minute read

DIA Europe 2022 : Reflecting on an insightful return to face-to-face conferences


minute read

Optimising Digital Transformation in Regulated Industries