Build Your Ideal Pharma Manufacturing City!

Here's a fun way to test your industry knowledge.

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.

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What percentage of pharma manufacturing process deviations are attributed to human error?

33%

10%

80%

17%

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Upwards of 80% of process deviations are attributed to human error.

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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."

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A primary objective is to align regulatory approaches and to harmonize international regulatory expectations and industry standards.

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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."

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Connected electronic batch records (EBR) let you seamlessly share information, alert users about patterns and issues, and mitigate quality events before they occur.

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Artificial intelligence (AI) is a necessary component to remain relevant in the pharma manufacturing industry.

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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."

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Accenture survey data cites that 75% of companies believe they risk going out of business if they don't scale to AI.

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A batch record can potentially contain over 40,000 entries.

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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."

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A biotech batch record can comprise 5,000 to 45,000 entries.

You are a pharma manufacturing ninja!

You have amazing insight into the future of pharma manufacturing, just like the many pharma companies setting themselves up for long-term success through digitization.

Get the blueprints for your modernized operation by downloading the trend brief “Pharma Manufacturing's Digital Journey.”

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