LAF, RABS, and Isolator Machines

The growing concern for product and operator protection, and the increasingly broad pharmaceutical regulatory framework make it essential to have available containment systems in conjunction with production equipment, should that be necessary.

In the aseptic pharmaceutical industry, manufacturing must be free of microbial and particle contamination. The environment classification required for aseptic or sterile processing is ISO 5 or class A, which requires:

  • Particle count (> 0.5 μm) less than 3,520
  • Suspended units per cubic meter
  • Laminarity of the flow covering the product
  • Humidity control
  • Temperature control
  • Air renewal
  • Cleaning and decontamination procedures

This set of standards have led Dara Pharma to develop a range of protection solutions ideal for any purpose and environment, delivering various levels of continuous protection with the following equipment:

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Dara Pharma designs, develops, and manufactures washing, sterilizing, filling, freeze-drying, and closing machines for vials, bottles, syringes, cartridges, and IV Bags to process liquid, semi-solid products, and powders in sterile conditions. NJM is Dara Pharma's exclusive representative in the U.S. and Canada.