Sumitomo Corporation

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Manufacturing

Prioritising patient safety with PMS

Effective as of 16 June 2025, the post-market surveillance (PMS) requirements mean that UK manufacturers must now have a robust process in place to monitor the safety and performance of medical devices after they are placed on the market
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Packaging

Adapting to the anticounterfeiting packaging landscape

Packaging specialist at Sumitomo (SHI) Demag UK, Ashlee Gough, examines the latest techniques being deployed to counteract infringements in the pharmaceutical sector and different methods to safeguard product and named-brand integrity
Manufacturing

Sumitomo Demag earns gold certification badge for emission-reversal

The company has earned a gold badge for its work in tackling emissions in comparison to other large British manufacturers and producers of CO2
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Salipro partners Sumitomo on pharmacological characterisations of drug candidates

The two companies have entered into a collaboration that leverages Salipro's platform technology to investigate the pharmacological characteristics of a compound from Sumitomo's programme
Manufacturing

Sumitomo (SHI) Demag expands own-brand robot range

Designed specifically for injection moulding machines, at K 2022 Sumitomo (SHI) Demag will reveal how it is accelerating its in-house automation platform
Finance

Sumitomo Demag launches subsidiary for Czech and Slovakian markets

Headquartered in Prague, David Svoboda has been appointed as MD of the company
Manufacturing

The value of validation

Validation exists to ensure that injection moulders have a stable and dimensionally centred process. However, it shouldn’t be regarded as a tick-box exercise just for medical moulders to test their tools to satisfy the FDA or other regulatory bodies
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