Life-sciences facilities operate under strict regulatory frameworks. Every pipe slope, every equipment clearance, every utility tie-in must be documented to a standard that holds up under FDA and EMA scrutiny. Scanning crews that don't understand validated environments are a compliance risk.
Our life-sciences practice is built on cleanroom-grade field protocols, GMP-aware documentation standards, and coordination workflows that integrate with CQV timelines. We've scanned active fill-finish suites, bulk API areas, and research labs without disrupting operations or violating environmental controls.
A defined deliverable package — scoped, fixed-fee, and documented for life sciences & pharma environments.
Deliverable 01
Existing-conditions scanning of cleanroom, lab, and process areas
Deliverable 02
LOD 350+ MEP coordination for clean utilities, process piping, and HVAC
Deliverable 03
Equipment clearance and rigging studies
Deliverable 04
As-built models structured for FDA/EMA audit documentation
Deliverable 05
Digital twins for facility lifecycle management
The technical edge cases that separate life sciences & pharma scopes from generic AEC engagements.
GMP-compliant field procedures and documentation
Cleanroom gowning and decontamination protocols
Coordination with CQV, validation, and process engineering teams
Background-suppressed deliverables for proprietary process areas
Plus the edge cases your facility will surface during scoping.
Tell us about your scope
Download a one-page PDF overview of our life sciences & pharma capabilities, deliverables, and engagement model.
Download Capability Sheet (PDF)BimCon Solutions delivers BIM coordination, 3D laser scanning, and MEP detailing for life sciences & pharma facilities. GMP-compliant scanning. Cleanroom and lab fit-outs. FDA-ready documentation.
BimCon Solutions
BIM · VDC · Reality Capture
GMP-compliant. Cleanroom-trained crews. Quote within one business day.
Response within one business day.
Confidential · NDA-ready · Nationwide deployment
