The repackaging in clean-rooms for starting materials is not yet requested by law but for many pharmaceutical companies it is an important requirement. At Hedinger we have continuously expanded our clean-room capacities over the years:
- 8 clean-rooms class D (100.000) for products with different characterics
- qualified according to EU-GMP
- continuous partical and microbiological Monitoring
- qualified personal (scientists, engineers)
- Clean-floor concept, where it is required.