Life Sciences Events & Webinars
The potential of truly digital, data-driven product labeling in life sciences is huge, allowing companies to tailor and update their information more readily, unencumbered by space restrictions or print/production line deadlines. But what will it take for today’s discrete, local pilot projects to evolve into something more permanent and transformational for patients and healthcare professionals?
Although the value of developing more data-driven processes is now widely recognized, many life sciences organizations today still routinely create critical documents and product labeling from scratch. This involves capturing and applying the same information repeatedly, yet often in different formats and using inconsistent terminology.
EMA’s latest shift in its IDMP implementation guidance has been well documented. At the coal face, it’s causing all kinds of confusion as pharma companies try to figure out what they should do now. At Amplexor BE THE EXPERT 2022, K2 Consulting’s Kelly Hnat will draw on her ‘insider’ knowledge as an active participant in the EMA SPOR Task Force and member of the EMA PMS Process Focus Group, to provide some welcome clarity.
At Amplexor BE THE EXPERT 2022 Steve Gens will unveil brand new research into what constitutes world-class and strong operational RIM performance, especially post pandemic, and explore how system and process developments are now giving way to organizational priorities such as data science investment, cross-discipline data governance, & strategic use of AI/automation tools.
GPRAS BERLIN CONFERENCE5 Essential IDMP Readiness Checkpoints for your Future-Proof RIM platformWatch this insightful presentation Renato Rjavec delivered at...
WEBINAR ON DEMANDEU IDMP Implementation: DADI and the agile way forward Beginning of this year, European Medicines Agency (EMA) has finally broken cover and...
WEBINAR ON DEMANDAmplexor Life Sciences Product Update: Q2/2022 Watch this customer-exclusive webinar where you’ll be able to learn about our recent product...
WEBINAR ON DEMANDNow that IDMP is real, is your RIM roadmap on the right track?After all the preparations for IDMP, it's here. But compliance will be a...
WEBINAR ON DEMANDChallenges and best practices for global patient engagementGlobal clinical trial success hinges on culturally appropriate patient engagement....
Find out how companies can approach IDMP data collection and quality challenges and decrease associated costs.
Find out how companies can improve business agility by producing and managing compliant, high-quality submissions in a cost and time-efficient manner.
Discover if your organization is on the right path to ensure long-term alignment with the demands of IDMP.
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