The medical device industry is changing fast, and for plastics companies, that means keeping up with a complex web of global regulatory frameworks and rigorous standards such as ISO 13485, EU MDR and FDA. These regulations and standards are not just red tape, they’re to ensure that materials, processes and finished products are safe, reliable…
RGE Group performed an initial ISO14001:2015 Gap analysis at itsWhittlesey and Alconbury sites and generated a detailed, comprehensive report, which…Read More
On 1 September 2025, Steffen Kroner, Arburg Managing Director Finance, Controlling, IT, Human Resource Management, and Director Apprenticeship Michael Vieth welcomed a…Read More
When running a business, cutting expenses is always on the table. Many owners look at insurance premiums as an area…Read More
Formerra, a leader in performance materials distribution, has announced an agreement with Epaflex S.r.l. that designates Formerra Europe…Read More
Plastics Training Online (PTO) has introduced four subscription tiers designed to provide manufacturers with greater flexibility and convenience in workforce…Read More
Sierra 57 Consult is a specialist Polymer Engineering Consultancy supporting clients across the UK, Europe, and Asia. Operating through four dedicated…Read More
Plastic migration, the transfer of chemical substances from plastic packaging into food or other products, is becoming a growing concern…Read More
Choosing the right injection moulder is one of the most important decisions you’ll make when developing a plastic product…Read More
Investing time and resources in keeping your injection moulding machinery in the best condition can eventually save you time and…Read More
