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Manufacturing, Packaging & Logistics In-Depth Focus 2019

Whether by ignorance of the latest best practices, or willful disregard for patient safety, the results of careless practice can often be fatal. The articles in this in-depth focus highlight how regulatory bodies are taking action to raise the industry’s game.

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    • Neil Piper offers a look at the global impacts of falsified and counterfeit medications in the light of the Falsified Medicines Directive’s (FMD) new requirements.
    • Jessica Clifton highlights the importance of considering certification to ISO 13485, by explaining the benefits for companies that manufacture medical devices and outlining how to achieve certification to this global standard.