Pharmaceutical Labelling

Labelling made simple

Managing Labelling documentation is a complex matter for Life Sciences companies, given not only the variety of the documents (Core Data Sheets through to individual labels for different dosage forms, strengths and markets), but also the need for managing translations, regulatory affairs interactions internally and with authorities, the changing industry regulations for such content, and the need to interact with Product Supply and integrate feedback loops from new safety / efficacy data and regulatory directives. CARA allows this complexity to be handled in a secure and simple way.