
Ready to Support EMA’s IDMP Implementation Guideline v2
Within a year, aligned and simultaneous document and data submissions will be live for Centralised Procedures managed by EMA, and pharma companies will need to

Within a year, aligned and simultaneous document and data submissions will be live for Centralised Procedures managed by EMA, and pharma companies will need to

The life sciences industry may have been slower than other markets to appreciate the benefits of holistic data and document management, but that is changing

Generis, the creator of the CARA™ foundational platform for content and business process management, has today announced new extensions to its Pharmaceutical and Medical Devices

3rd Feb, 2021, London, Generis, a leader of world-class, cloud-hosted content and regulatory information management solutions, today announced a strategic global partnership with Data Conversion Laboratory (DCL), enabling life

Let’s take a look at that last one: cost-efficiency. With the economic impacts of nations favouring isolationism amid the ongoing pandemic, many businesses are looking

So far this year, Generis has bolstered its already deeply-experienced Life Sciences business development team with the appointment of Stefan Rupp, formerly VP of Global
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