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"
The leading cause of drug shortages is supply disruptions due to quality or manufacturing issues.
See how a digitized quality management solution gives you an intelligent approach to quality and compliance. Download the trend brief "Adapting to Pharma's Next Normal."
63% of the drug shortages stem from quality and manufacturing issues.
What percent of lead time is attributed to using manual processes and paper records?
See how to implement quality assurance (QA) procedures at each phase of the production line and minimize errors. Download "The Ultimate Guide to Digitizing Pharma Manufacturing."
30% to 70% of manufacturing lead time is mainly due to manual processes, disconnected instruments, and non-standard paper-based documentation and control procedures.
"Dare to be Different: It's Time to Revamp Collaboration in Life Sciences Contract Manufacturing," Accenture Life Sciences.
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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