Sector · Pharmaceutical Manufacturing & Cleanrooms

Fire, security & ventilation
for Pharmaceutical Manufacturing & Cleanrooms.

In a pharmaceutical plant, a fire seal is an atmospheric seal — fire stopping must hold ISO 14644 pressure cascades as well as smoke. Aspirating detection copes with the high air-change rates of classified suites. Inert gas suppression leaves no residue near bioreactors, verified by annual room integrity testing. Airlock interlock logic on access control preserves pressure zones, and every maintenance visit runs clean-in, clean-out. MHRA and EU GMP Annex 1 scrutiny means a particulate breach is a batch loss.

What we deliver here

Service lines for pharmaceutical manufacturing & cleanrooms.

Why it matters now

Where the compliance
pressure is.

MHRA and EU GMP Annex 1 inspection regime · ISO 14644 suite classification · Batch loss risk from particulate or residue contamination · Annual room integrity testing · Clean-in, clean-out maintenance protocol.

Standards we design to

The regulations
that shape the work.

  • EU GMP Annex 1 (sterile medicinal products)
  • ISO 14644 (cleanroom classification)
  • MHRA GMP inspection regime
  • BS 5839-1 (aspirating detection)
  • BS EN 15004 (inert gas suppression and room integrity testing)
  • Regulatory Reform (Fire Safety) Order 2005

Every install is delivered to the relevant British / European standard with an audit-ready evidence pack at handover.

Talk to us

One call covers
the whole building.