Hedinger GMP/GDP System

Clean-room repackaging

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.