Cleanroom contractor for Kazakhstan: design, supply and installation

By ZY Cleanroom · Updated 2026-11-01 · Sources at the end of the page

What ZY does for a project in Kazakhstan

ZY designs cleanrooms and makes the cleanroom panels and doors in its own factory in Tianjin, China. The air system, windows, air showers and pass boxes are supplied in the same quotation. Choose turnkey, design and supply, or supply only.

Site work is delivered with a licensed local contractor named in the contract: yours, or one agreed with you. ZY supplies numbered drawings, an installation guide, remote video support for set-out and the first panels, and on-site supervision for larger projects.

Panels are cut to length, numbered to the layout drawing and packed on timber pallets in Tianjin. Give us the site city and we plan the route. Send a room list or floor plan for a first scope and budget range.

The rules below decide what your facility needs; your regulator approves the facility.

Which rules apply to your facility

Order No. ҚР ДСМ-9 says inspections check sites against national standards and/or the EAEU GMP Rules. A GMP certificate is issued after inspection and is valid for three years (Adilet, checked 31 October 2026).

The sanitary rules cover lighting, ventilation, air conditioning, heating, room repair and medical waste in health facilities (Adilet, checked 31 October 2026).

Who builds cleanrooms here

Under these texts, two groups need cleanrooms: makers of medicines, who need a GMP certificate, and health facilities, which follow the sanitary rules. Both answer to the Ministry of Healthcare.

PIC/S status and the GMP text

Kazakhstan applied to join PIC/S on 20 March 2025. PIC/S confirmed the application complete in November 2025 and announced it on 10 February 2026. The applicants are the Committee for Medical and Pharmaceutical Control and the National Center for Expertise of Medicines and Medical Devices (PIC/S, 10 February 2026). Kazakhstan is not yet on the PIC/S member list.

The order also covers remote and outsourced inspections and includes a template for an EAEU GMP certificate (Adilet, checked 31 October 2026).

What to send for a first scope

Send the room list with the ISO 14644-1 class and occupancy state for each room. Add floor plans and ceiling heights. State whether the owner seeks a GMP certificate under Order ҚР ДСМ-9 or works under the health facility sanitary rules.

Send your room list to ZY Cleanroom, a cleanroom design-and-build contractor with its own panel factory in Tianjin, China, to have a first scope prepared. Certification and testing can be arranged per project.

Who does the site work

Site work is delivered with a licensed local contractor: yours, or one named in the contract. ZY supplies the design, panels, doors and numbered drawings.

Related guides

• What a cleanroom costs to run: energy, filters and testing
• Writing a cleanroom URS: contents and testable wording
• How to Import a Cleanroom from China
• The Cleanroom Project Lifecycle
• Turnkey cleanroom contractor
• Room list builder

Sources

• Adilet, Order of the Minister of Healthcare No. ҚР ДСМ-9 of 27 January 2021, Rules for Conducting Pharmaceutical Inspections on Good Pharmaceutical Practices (checked 31 October 2026)
• Adilet, Order No. ҚР ДСМ-96/2020 of 11 August 2020, Sanitary Rules for health facilities (checked 31 October 2026)
• PIC/S, Kazakhstan applies for PIC/S membership (10 February 2026)