Pharmaceuticals / life sciences
Information processes without risks and side effects
Pharmaceuticals, life sciences and medical technology are among the most highly regulated industries in the world. Therefore, one of the key challenges is pushing new products through the necessary approval processes of the relevant authorities, such as the EMA, FDA, PMDA and SFDA.
In addition to medical and clinical aspects, consistency in the submitted documentation plays a key role: Consistency of content, formulations and terms in clinical studies, accompanying documents, R&D documents and similar documentation avoid time-consuming queries and costly correction loops, thereby considerably reducing the time to market.