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.
Service lines for pharmaceutical manufacturing & cleanrooms.
Fire Systems
Fire alarms and evacuation, AOV smoke extract, disabled refuge and PAVA. Designed, installed and maintained to current British standards, with monitored response when the alarm actually sounds.
Gas Suppression Systems
Inert and chemical gas suppression: design, install, repair and maintenance for data centres, comms rooms and irreplaceable assets.
Passive Fire Systems
Fire doors, fire stopping, compartmentation, barriers and risk assessments: the protection that works without anyone pressing a button.
Ventilation & Air Quality
AHU and ductwork install, service and repair, fire-damper testing, ventilation hygiene, AOV smoke extract, air conditioning and commissioning.
Security & Access Control
Intruder alarms, CCTV, access control, door entry and 24/7 monitoring: the systems that stay awake after the last person leaves.
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.
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.