Cleanroom

Rosti Group will attend Medical Manufacturing Asia 2026. Held biennially  Medical Manufacturing Asia brings together healthcare professionals medical device

For manufacturers of medical devices, diagnostics and pharmaceutical products, selecting the right cleanroom classification is critical. The wrong choice can increase cost, delay validation and create unnecessary compliance risks. While cleanroom injection moulding is essential for controlling contamination, not all cleanrooms offer the same level of environmental control

Successful medical device manufacturing requires a partner with expertise in Design for Manufacture (DFM), validation, automation, cleanroom manufacturing and global supply chain management. Leading medical manufacturers increasingly seek partners that can support the entire product lifecycle, from concept to reality of high-volume production.

We have announced the official launch of a new ISO Class 8 (Class 100,000) medical cleanroom at our China facility, further strengthening the Group’s global capabilities in high-precision medical manufacturing.

New cleanroom investments strengthen Rosti’s support for regulated medical and life sciences customers and position the company for continued growth

Rosti is making significant investments in medical plastic injection moulding and cleanroom production capabilities across Europe Asia and North America

Rosti Group is delighted to announce that we will be exhibiting at MedTec China 2025 taking place from 24–26 September…

As a leading precision plastic injection moulding business Rosti knows that quality is non-negotiable — for us and for our…

As part of Rosti Group’s growth strategy and continuous investment in our capabilities we are delighted to open our new…