Segment 01 · APS
Aseptic Processing Systems
Barrier isolators, RABS, vial and syringe filling lines, depyrogenation tunnels and production lyophilisers. Our largest segment by revenue and by service hours.
Pharmaceutical & Medical Equipment · Singapore · Since 2004
The machines that make medicine provable.
We build the aseptic, solid-dose and sterilisation equipment that manufacturers across Asia validate, qualify and run for twenty years. Every machine ships with the evidence to prove it works.
Filling zoneISO 5at rest
Δp · Grade A→B0.0Pa
Air temperature0.0°C
Relative humidity0%RH
≥0.5 µm count0/m³
What we do
Founded2004 · Singapore
SegmentsFour
PlatformsTwelve
Installed3,100+ units
Markets24 countries
Export ratio78% of revenue
A pharmaceutical plant is only as good as the evidence behind it.
DeepMedic Pharma is a capital equipment manufacturer. We do not make drugs — we make the machines that make them, and the documentation that lets a regulator believe the result.
That distinction shapes everything. A tablet press is a mechanical problem. A validated tablet press — one whose every weld, sensor and firmware build can be traced, challenged and re-qualified years later — is an engineering and evidentiary problem at once. We treat it as one job, not two.
From our Toa Payoh headquarters, our Tuas and Jurong plants, and our fabrication centre in Johor, we supply aseptic processing, solid-dose, sterilisation and inspection systems to pharmaceutical manufacturers, CDMOs, biologics developers and hospital pharmacy groups across the Asia–Pacific.
Our business
Four segments,
one engineering base.
The segments share a machine shop, a controls team and a validation department. That is why a sterilizer and an isolator from us behave the same way in a document set — and why a plant can qualify both against one protocol library.
Segment 02 · SDT
Solid Dose Technologies
Rotary tablet presses, fluid-bed granulators, capsule fillers, coaters and blister lines — containment-rated to OEB 4 for potent compounds.
Segment 03 · SUE
Sterilisation & Utilities
Pharmaceutical steam sterilizers to EN 285, WFI generators, pure steam generators and clean utility distribution built to ASME BPE.
Segment 04 · IDS
Inspection & Digital
Automated visual inspection, leak detection, serialisation and aggregation, plus the MES connectors that make Annex 11 and Part 11 compliance routine.
Selected platforms
Built to be
re-qualified.
Twelve production platforms, each with a documented change history going back to first release. Nothing here is a one-off.
DM-IS 700Aseptic Processing
Aseptic Barrier Isolator
Closed-loop VHP bio-decontamination with a validated 6-log cycle in under 90 minutes. Grade A over the full working aperture.
DM-TP 45Solid Dose
Rotary Tablet Press
45 stations, 320,000 tablets/hour, with per-tablet compression force logged and retained for the full batch record.
DM-SR 12Sterilisation & Utilities
Pharmaceutical Steam Sterilizer
EN 285 double-door pass-through, 12 m³ chamber, F₀-controlled cycles with independent redundant probes.
FY2025 in figures
Growth we can
account for.
Audited results for the year ended 31 December 2025. Full statements and the FY2025 annual report are in Investor Relations.
412.6S$MRevenue+11.4% year on year
14.3%Operating marginS$58.9M operating profit
7.6%R&D intensityS$31.2M invested
1,180EmployeesAcross six countries
Quality & regulatory
QMSISO 13485:2016
QualityISO 9001:2015
EnvironmentISO 14001:2015
SafetyISO 45001:2018
SterilizersEN 285
SoftwareGAMP 5 / Part 11
PipingASME BPE
Audits FY2531 client · 4 notified body
We are audited so that our customers pass theirs.
Thirty-one customer audits and four notified-body assessments in 2025. None resulted in a critical finding. That number is the product we are actually selling.
Every DeepMedic machine ships with a qualification package built for the regulator who will read it: design specification, traceable material certificates, FAT and SAT protocols, calibration records, and a software build hash tied to the serial number. When your inspector asks a question in 2034, the answer is already written down.
Sustainability
The cleanroom is the problem.
A Grade B suite runs its air 24 hours a day, forever. It is the single largest energy load our customers carry, and the one place our engineering can move the number. Our current isolator platform cuts conditioned-air demand by up to 38% against the open-RABS layout it replaces.
Careers
Engineering you can point at.
We hire controls engineers, validation specialists, welders certified to ASME IX, and field service engineers who like aeroplanes. You will be able to walk into a plant in Hyderabad or Songdo and say which machine is yours.
Newsroom
Latest.
02 Jul 2026ProductDM-IS 700 gains third-party validation of a 6-log VHP cycle at 88 minutes, cutting changeover on multi-product filling lines
19 Jun 2026Investor1H FY2026 business update: order book at S$268M, Aseptic Processing Systems up 17% on biologics demand
28 May 2026CorporateSenai fabrication centre completes 24,000 m² expansion, adding ASME IX orbital welding capacity
14 Apr 2026SustainabilityFY2025 Sustainability Report published: Scope 1 and 2 emissions down 9.2% against a 2022 baseline
Talk to an engineer
Send us the URS. We will send back a real answer.
Not a brochure. A named application engineer, a line layout, a cycle estimate and an honest view of whether we are the right supplier for it.