Shanghai Xuwill Automation Equipment Co., Ltd.

Pharmaceutical equipment and cleanroom engineering, delivered as one project

From solution preparation and aseptic filling to cleanroom construction, robotics and life science bioprocessing — Xuwill supplies, integrates and validates the complete production line.

Robotic vial handling on an aseptic filling line
Founded 2013Shanghai-based engineering team
cGMP & Annex 1Designed for regulated markets
Turnkey EPCDesign, build, install, qualify
Worldwide DeliveryInstallation and after-sales support

What we supply

Five equipment divisions under one supplier

Instead of coordinating a dozen vendors, you deal with one engineering team that understands how the whole line has to fit together.

GMP cleanroom production suite

Turnkey EPC

We build the room as well as the machine

A filling line is only as good as the environment around it. Xuwill designs the facility, models it in BIM, installs the HVAC and utilities, sets the equipment and runs the qualification — so responsibility for the finished suite sits with one party.

  • Facility layout, personnel and material flow design
  • Full BIM coordination with clash detection before construction
  • HVAC, purified water, clean steam and process gas systems
  • FAT, SAT, commissioning and IQ/OQ/PQ documentation
Cleanroom EPC Solutions
Analytical instrument laboratory

Life science & laboratory

From seed vial to finished drug product

Our life science division covers the full cell and gene therapy workflow — cryopreservation, seed cultivation, single-use bioreactors, purification, harvest and drug product filling — together with the media, bags and consumables that keep it running.

For laboratories working to a budget we also supply inspected, refurbished chromatography and mass spectrometry systems from Shimadzu, Agilent, Thermo Fisher and Waters, each supplied with a performance report.

Life Science & Bioprocess

Why Xuwill

Built for regulated manufacturing

One point of responsibility

Equipment, cleanroom and integration are contracted together, so nothing falls between suppliers when the schedule tightens.

Documentation that passes audit

URS, DQ, FAT, SAT and IQ/OQ/PQ packages prepared to cGMP, EU GMP Annex 1, FDA and NMPA expectations.

Configured, not catalogued

Every line is sized to your product, output, container format and target market rather than sold from a fixed spec sheet.

Support after handover

Spare parts, remote diagnostics, operator training and on-site service wherever the equipment is installed.

Tell us what you need to produce

Send your URS or a short description of the process — product, output per hour, container format and target market. Our engineers reply with a technical proposal and budget price within one working day.

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