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C2 Cleanroom Pharmaceutical Sector IconTypical processes:

  • Blister packing
  • Contract manufacturing
  • Tablet manufacturing
  • Two-piece encapsulation
  • Powder handling


As highly regulated as the medical markets, pharmaceutical markets need to keep quality at the forefront of cleanroom facility design.

ISO Class 5 (EU GGMP Grade A/B) mini environments or integrated laminar flow areas will protect critical processes, whilst the rest of the cleanroom can cope with a lower quality of air keeping running costs low. EU GGMP will be cross referenced to the ISO 14644-1 standard.


Another area to consider when preventing cross contamination is containment with continuous environmental monitoring where applicable. The velocity of the extracted air is designed to contain all airbourne particles and provide a safe operating environment for personnel. Ideal for powder handling, weighing, purity testing, chemical analysis and packaging.

Our Pharma Clients

Pharmaceuticals is such an important sector to Connect 2 Cleanrooms and our cleanroom solutions play an integral part in many healthcare companies who work to enhance the quality of our lives.




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