Your journey into the future of pharma development begins here. Build a fully modernized and highly profitable pharma manufacturing city by completing this 5-question quiz. Each correct answer adds a structure and brings you closer to your optimal pharma manufacturing ecosystem.
What percentage of pharma manufacturing process deviations are attributed to human error?
See how to create productive connections between people, processes, and systems. Download the case study "How Modernizing Operations Gave QuVa Pharma a Stronger Competitive Edge in the Pharmaceutical Market."
Upwards of 80% of process deviations are attributed to human error.
Ginette Collazo, Ph.D. "Eliminating Human Error From Your List of Manufacturing Deviations"
Which of the following is not an objective of the FDA's Digital Health Center of Excellence?
See how to adopt new data-driven approaches to manufacturing management and data sharing. Connect and align quality and production across your company's ecosystem. Download the trend brief "Adapting to Pharma's Next Normal."
A primary objective is to align regulatory approaches and to harmonize international regulatory expectations and industry standards.
"Digital Health Center of Excellence," U.S. Food and Drug Administration (FDA), Feb. 2022.
The timeline required for clinical trials is often the key element to achieve faster time to market. How can your company achieve this?
See how to more effectively manage, link, track, organize, and store all essential electronic trial master file (eTMF) materials. Download "The Ultimate Guide to Digitizing Pharma Manufacturing."
Connected electronic batch records (EBR) let you seamlessly share information, alert users about patterns and issues, and mitigate quality events before they occur.
Artificial intelligence (AI) is a necessary component to remain relevant in the pharma manufacturing industry.
See how predictive analytics helps you make more accurate predictions about future or otherwise unknown events. Download "Shaping the Next Normal for Quality and Compliance."
Accenture survey data cites that 75% of companies believe they risk going out of business if they don't scale to AI.
"AI: Built to Scale," Survey Report, Ketan Awalegaonkar, Robert Berkey, et al., Accenture Life Sciences.
A batch record can potentially contain over 40,000 entries.
Numerous batch record entries are time-consuming and error-prone. Find out how a fully connected, digital manufacturing solution creates paperless and error-free records. Download the e-book "Connecting and Leveraging Quality-Driven Data Throughout the Pharmaceutical Product Life Cycle."
A biotech batch record can comprise 5,000 to 45,000 entries.
"Operations Can Launch the Next Blockbuster in Pharma," Ulf Schrader, McKinsey & Company, Feb. 16, 2021.
Get the blueprints for your modernized operation by downloading the trend brief “Pharma Manufacturing's Digital Journey.”
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