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Pharmaceutical Manufacturing and Packing Sourcer

Perfect Packaging

Far too frequently, life sciences brands have to withdraw products from the market at great cost and risk to their reputation. This is usually because errors have slipped through, which could impact patient safety. Why is this still happening, and what is needed to ensure companies get high quality, compliant products onto the market promptly and efficiently? This article explores the challenges and charts a way forward.

In this age of automation, it seems astounding that some fundamental tasks, such as packaging and labelling quality checks, are still handled manually, at least to some degree. This is the case, even among some of the biggest pharmaceutical brands, despite the high regulatory standards designed to protect patients, the reputational risks, and steep costs if errors slip through the net.

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Marc Chaillou is Regional Sales Director at Schlafender Hase, a company that provides intelligent proofreading software, managing key accounts and collaborating with sales partners in export markets. Before joining the company seven years ago, he worked in business development roles at technology market analysts Gartner and Datamonitor. Marc speaks four languages fluently: French, English, Spanish, and German.
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