Guest contributor Peter Brandstetter explains why a digital approach to content control is the way forward for life sciences companies.
Becoming ‘IDMP ready’ is a marathon, not a sprint: the most important factor for compliance is being on the right path. So what’s your starting point?
Life sciences companies may have regulatory information management systems, but are they being used to their full potential?
With EU IDMP 2.0, life sciences companies need to be on the lookout. Check how you can maximize efficiency of your regulatory submission processes.
Virtual and augmented reality technology continue to develop and improve at a rapid pace. Here’s how it can be useful for life sciences.
With the publication of EMA’s IDMP/SPOR implementation guide (V2), the transition of the ISO IDMP product data standard can be transformational.
On 22nd February 2021, the long-anticipated moment happened: the European Medicines Agency (EMA) has published the EU IDMP Implementation Guide version 2.
The year 2020 saw a wide range of Amplexor thought leadership in pharma titles around the world. Here’s a look back.
Robotic Process Automation (RPA) is increasingly seen as a solution to laborious, repetitive, resource-draining document and data processing.
In the years to come, life sciences firms should shift their attention to new, improved RIM solutions. Here’s what’s next in RIM.
Amplexor’s annual Be The Expert, traditionally a traveling conference, took place in a totally different way this year: virtually. Here’s how it went.
How can richer, more holistic product information – compiled in response to regulatory requirements – help transform life sciences business outcomes?
Discover our Life Sciences solutions
Connect with us today!