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Manufacturing
Quality management during manufacturing changes: part II
In the second part of this article, the authors delve deeper into how effective change management enables pharmaceutical manufacturers to handle the challenges and risks of rapid, simultaneous industry shifts, thereby ensuring that quality and patient safety remain uncompromised throughout the process
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Manufacturing
Quality management during manufacturing changes: part I
Change is a universal constant and continues to accelerate in the realms of pharmaceutical, medical device and in-vitro diagnostic manufacturers who face ever-increasing pressure to optimise costs while maintaining high product quality and patient safety standards
Regulatory
How to proactively address EU HTAR implementation challenges before 2025
Data landscape challenges within the European Union (EU) have historically been driven by the different laws, processes and regulatory standards of its 27 member states (MS). As a result, drug therapeutics and health technology developers have faced the challenge of duplication of assessment efforts
Drug Delivery
IQVIA discusses supply chain resilience for CPhI Discover
Informa’s CPhI Discover virtual event is taking place from 17-28th May, and the company recently spoke with Aurelio Arias, Engagement Manager, Thought Leadership at IQVIA ahead of a session he is moderating on the ‘API Landscape, Reshoring and sourcing dynamics’. (Thursday 20th at 3pm CET)