Navigating data management challenges in the pharmaceutical life cycle

In this webinar, we introduce you to laboratory information management systems (LIMS) and demonstrate how this software can help you achieve regulatory compliance, quality data management throughout your product’s life cycle.
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OTHER ON-DEMAND WEBINARS

Realizing The Opportunity To Increase Quality And Improve Efficiency Of Safety Data Collection Within Patient Support Programs

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Patient Support Programs (PSPs) have changed dramatically over the past decade; they have become global activities, and grown significantly in scale and complexity. While PSPs are also an increasingly valuable resource for pharmacovigilance due to the extensive patient safety data they generate, they have suffered from the traditional lack of standardized mechanisms for recording, reconciling and managing this data, resulting in resource heavy processes, and a lost opportunity for deeper product understanding for Pharma. Fortunately, new technologies are helping to tackle this challenge.
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Automation in Biopharma and the Impact on Workflows

In this exclusive Drug Digest video interview, Meg Rivers and Feliza Mirasol, Pharmaceutical Technology editors, discuss the benefits of automating entire workflows in analytics versus automating only specific pieces of equipment or only certain processes with Nick Pattinson, head of product, Automata.
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WEBINAR Improve efficiency and return on investment by adopting molecular spectroscopy techniques in pharma manufacturing

In this on-demand webinar, discover the differences between FTIR, NIR and Raman spectroscopy, learn how spectroscopy is applied in quality control labs and hear how implementation of these techniques increased efficiency and minimised costs.
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Covid Vaccines & Beyond - mRNA vaccine future uses and the role of excipient lipid nanoparticles

Registration fees are refundable for attendees registered for individual webinars, if cancellation is received at least five (5) business days prior to the course.
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