Containment requirements in the pharmaceutical industry today

Manufacturers of pharmaceutical production machines:

• They generally meet the today set requirements
• However, only during handling of their machines when they are turned off.
• Protection of operator
• Purity of product
• Avoidance of cross-contamination
• Maintaining of set room pressures in production rooms at all times
• Compliance with GMP requirements of production machines
• Providing of units which can be validated
• Documentation of all production relevant activities

“What makes us different is that we listen to our clients, work according to their needs and deliver a product well beyond their expectations.”

How does contamination take place?
How get active compounds into the human body?
Is a breathing mask sufficient?

• Lungs
• Eyes
• Mouth
• Skin

Manufacturers of laminar flow cabins and isolators

• concentrate on manual handling processes with low dust concentrations

Manufacturers of pulse jet filter systems have little to offer to the needs of pharmaceutical industry in regard to:

• Filtration and dust recoveryof submicron dust particles and aerosols effectively
• complyance with containment and explosion prevention dealing with organic
  substances