Dual and multi-sourcing strategies for medical device manufacturers How do you actually implement dual or multi-sourcing without introducing new risks around validation, cost or compliance? 31 March, 2026 More
EU Medical Device Regulation - traceability by design and the importance of building compliance into every medical component 10 March, 2026 More
How important is multi-sourcing in medical device manufacturing? Many medical OEMs are increasingly exploring multi-sourcing strategies when planning their manufacturing operations. 26 February, 2026 More
What is ISO-13485 compliance-by-design? Forward-thinking manufacturers are adopting a compliance-by-design mindset by embedding ISO 13485 principles from day one. 12 February, 2026 More
What are the benefits of small wave springs? Wave springs have the potential to address many of the challenges faced by modern medical device designers. 15 January, 2026 More
What are the best spring materials for pharmaceutical products? A pharmaceutical spring faces stricter manufacturing and compliance requirements than most other spring applications. 07 January, 2025 More
How to reduce the risk of particulates in medical manufacturing Medical devices face an array of stringent regional and international regulatory measures. 17 December, 2024 More
How the design of pharmaceutical springs determines fatigue life The fatigue life of springs determines their long-term reliability to actuate with a desired amount of force before they.. 10 December, 2024 More
A guide to design for manufacture in pharmaceutical products A guide to better quality outcomes, minimising scrap rates, eliminating rough edges and volume manufacturing in the medical.. 28 November, 2024 More
What causes spring entanglement in pharmaceutical manufacturing? Entanglement is the result of spring coils becoming interlocked and compromising a spring’s ability to actuate. 28 February, 2024 More