Cleanroom contractor for Uzbekistan: 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 Uzbekistan

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

Decree UP-137 of 19 August 2025, in force from 23 August 2025, governs the circulation of medicines and medical devices. From 1 January 2026, domestic and foreign manufacturers need the national certificate "Good Manufacturing Practice - GMP" to register a medicine or extend its registration. Medicines that passed WHO prequalification and are registered by recognition are excepted (Decree UP-137, clause 4(a), Lex.uz).

From 1 January 2027, a certificate of conformity for a medicine requires the manufacturer's national GMP certificate for that type of medicine. For devices, the manufacturer's certificate of conformity to the national ISO 13485 standard is required from 1 July 2027 (Decree UP-137, clause 5, Lex.uz).

For hospitals, a presidential resolution of 5 May 2026 moves licensing of medical organisations to a Center for Licensing and Accreditation of Medical Organizations from 1 July 2026. It orders the Ministry of Construction to revise design, construction and commissioning standards for medical facilities within three months (UzDaily, 5 May 2026). Ask the owner which version applies.

Who builds cleanrooms here

Medicine and device makers are the regulated buyers, because the decree ties their certificates to GMP and ISO 13485. Hospitals are the other group. The same licensing standards will apply to public and private clinics, and more than 3,000 state medical institutions must meet licensing requirements by 2030 (Kun.uz, 6 May 2026).

What a foreign contractor must arrange

The law firm GRATA International says Uzbek licensing law does not stop foreign companies from applying for design and construction licences. A licence given to a non-resident creates a permanent establishment for tax, to be registered within 180 days of issue. Foreign staff of a local permanent establishment or subsidiary need a work permit from the Uzbekistan Agency for Foreign Labour Migration, and local companies are often needed in practice for hiring and equipment imports (GRATA, 18 September 2024). Agree with the owner who holds the licence.

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 plant makes medicines or devices, whether the rooms are sterile or non-sterile, and which certificate date the owner works to. For a hospital, say whether it is public or private.

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

• How to audit a cleanroom panel factory, on site or by video
• What a cleanroom costs to run: energy, filters and testing
• Writing a cleanroom URS: contents and testable wording
• How long does it take to build a cleanroom?
• Turnkey cleanroom contractor
• Room list builder

Sources

• Lex.uz, Presidential Decree UP-137 of 19 August 2025, circulation of medicines and medical devices (checked 1 November 2026)
• UzDaily, Uzbekistan sets sweeping healthcare quality reform standards (5 May 2026)
• Kun.uz, Uzbekistan to tighten oversight of medical clinics and introduce new accreditation requirements (6 May 2026)
• GRATA International, GILS Construction and Infrastructure: Uzbekistan (18 September 2024)