From Funding to First GMP Batch
We Deliver the Entire Facility Lifecycle
Funding → Build → Qualify → License → Manufacture
From Funding to First GMP Batch
We Deliver the Entire Facility Lifecycle
Funding → Build → Qualify → License → Manufacture
Need to build a licensed pharmaceutical facility?
We lead from concept to compliant commercial batch, eliminating delays and regulatory risk.
From Funding to First GMP Batch
We Deliver the Entire Facility Lifecycle
Funding → Build → Qualify → License → Manufacture
From Funding to First GMP Batch
We Deliver the Entire Facility Lifecycle
Funding → Build → Qualify → License → Manufacture
Need to build a licensed pharmaceutical facility—fast, funded, and inspection-ready?
We lead from concept to compliant commercial batch, eliminating delays and regulatory risk.
The Problem:
You’re not short on ambition or funding. But most GMP facility projects fail for the same reasons:
- No single partner owns the full lifecycle: Funding → Build → Qualification → License → Manufacture
- Design and construction vendors move fast—without a regulator-facing lead in the room.
- Internal QA teams are overrun or looped in too late.
- Licensing timelines are vague—and slip by 6 to 12 months.
- You spend millions building, then stall due to compliance issues.
Every delay erodes investor confidence, market access, and credibility with regulators.
2040 Consulting prevents that drift by owning the entire lifecycle
from feasibility to first GMP batch.
What We Do:
Capital sourcing and investor-facing materials
Full regulatory license delivery (MOHAP, EDE, FDA, EMA)
Design & Construction partner selection
Land & free zone strategy (DSP, DIC, DHCC, JAFZA)
Cleanroom, utility & CQV oversight
Compliant commercial batch readiness
Whether you're building a sterile injectables plant, a biotech scale-up site, or a multi-phase hub, we drive the entire process.
Who This Is For:
This service is ideal if you are:
Government entities or industrial ministries
localizing pharmaceutical manufacturing
Sovereign wealth funds or state investors
backing regulated healthcare infrastructure
VC and private equity firms
focused on life sciences or biomanufacturing
Healthcare angel investors
co-developing strategic pharma assets
Consultancies or project firms
needing GMP-qualified delivery leadership
Real estate developers
planning life sciences zones or pharma clusters
Pharma, biotech, or CDMO companies
expanding into UAE or MENA manufacturing
Why Clients Choose Us:
$500M+ in capital projects delivered
(OSD, sterile injectables, drug–device combinations)
Regulatory standards met
across US, EU & UAE—with zero critical observations
Ability to deploy GMP expertise rapidly
Previously deployed 30 consultants across 3 continents in 14 days
20+ years GMP, QP/RP-eligible, PMP-certified
Personally led by PJ Murphy
Looking for other GMP support outside a full facility build?
Looking for operational or QA/QC support outside a full facility build?
Ready to Build with Speed, Clarity & Compliance?
Book a free 15-minute Feasibility Call
to learn how we deliver GMP facilities—on time, on budget, and inspection-ready.