Cleanroom

For manufacturers of medical devices, diagnostics, and pharmaceutical products, choosing the right cleanroom classification is crucial. Making the wrong choice can lead to higher costs, validation delays, and unnecessary compliance risks. While cleanroom injection molding is essential for contamination control, not all cleanrooms provide the same level of environmental control.

Successful medical device manufacturing requires a partner with expertise in Design for Manufacturability (DFM), validation, automation, cleanroom manufacturing, and global supply chain management. Leading medical manufacturers increasingly look for partners who can support the entire product lifecycle, from concept through to 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 molding and cleanroom production capabilities across Europe Asia and North America

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

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

As part of Rosti Group’s growth strategy and ongoing investment in our capabilities we are excited to announce the opening…