Portescap’s business development manager for medical applications, Dave Beckstoffer, explains how drive systems for wearable and automatic drug delivery devices are central to the patient outcome.
ArisGlobal’s director of product management’s Agnes Cwienczek, reports on AI-boosted regulatory process automation and other top-level findings from a new Censuswide survey of senior life sciences regulatory professionals.
While it officially applies to the manufacture of sterile medicinal products in the European Union, the revised EU Good Manufacturing Practice (GMP) Annex 1 effectively reset the benchmark for quality standards across the globe.
Stefan Karl, CEO, Mikrobiologisches Prüflabor, Innsbruck and Olaf Degen, director industry microbiology, Bruker Microbiology & Infection Diagnostics discuss how advanced microbial ID systems accelerate product release testing.
Ian Loudon, international sales and marketing manager at alarm annunciator specialist Omniflex, explores the importance of alarm annunciators in monitoring the temperature in pharmaceutical and laboratory environments.
Koki Obara, marketing manager, Asahi Kasei Medical, delves into the current biopharmaceutical environment, the critical role of virus removal filters, and how Planova FG1 stands to impact the development and production of biopharmaceuticals.
After IFPMA, GSCF, and IGBA submitted a joint opening statement at the fifth session of the Intergovernmental Negotiating Committee (INC-5), European Pharmaceutical Manufacturer spoke to Melchior Kuo, manager, Innovation and Vaccine Policy, IFPMA.
After hearing the news of Cytiva and Syvento Bitotech's new facility, European Pharmaceutical Manufacturer followed up with Ludovic Brellier, president of Hardware Solutions at Cytiva, for more information.
