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Contact Info

Phone number

92 321 8073738

Email address

info@pakgusu.com

Address info

8-Km, Sundar-Raiwand Road, Lahore, Pakistan

Dammam and the wider Eastern Province sit at the heart of Saudi Arabia's industrial corridor — a dense cluster of petrochemical complexes, electronics and semiconductor assembly, and a fast-growing pharmaceutical and medical-device base stretching across Dhahran, Khobar, Jubail and Ras Tanura. These sectors share one demand: tightly controlled, particle-stable environments that hold their classification through long, humid Gulf summers. Pak Gusu, a Pakistan-based cleanroom manufacturer and technical partner of GUSU Purification (China), designs and builds modular cleanrooms for exactly these applications and ships them into the Eastern Province.

We do not operate a Dammam office, and we are direct about that. What we offer is engineering, fabrication and a validation-ready cleanroom delivered to your site — with optional on-site installation and supervision at additional cost. Every system is designed to meet ISO 14644 and, for sterile pharma and aseptic processing, EU-GMP Annex 1 (Grade A/B ≈ ISO 5, C ≈ ISO 7, D ≈ ISO 8). The result is a cleanroom that arrives compliant by design and ready for your SFDA submission, not a promise we cannot keep locally.

Why Dammam-Based Manufacturers Choose Pak Gusu

The Eastern Province is unlike Riyadh or Jeddah in its industrial mix. Alongside Aramco-anchored petrochemical and energy activity, the region hosts electronics and semiconductor lines that need low-particle, ESD-aware environments, plus a maturing pharma and medical-device cluster serving the Kingdom. Each of these needs a different cleanroom recipe, and we build to the brief rather than to a catalogue.

Our Eastern Province clients typically need one or more of the following, and our modular systems are designed for all of them:

  • Pharma and sterile-fill suites — EU-GMP Annex 1 Grade A/B/C/D layouts, validation-ready for SFDA review
  • Medical-device assembly and packaging — ISO 7 / ISO 8 rooms aligned with ISO 13485 quality systems
  • Electronics and semiconductor work — ISO 5 to ISO 7 environments with ESD flooring and low-shedding finishes
  • QC and microbiology laboratories — controlled, GSO-compliant testing spaces

Because the structure is modular — sandwich-panel walls, flush cleanroom doors and windows, integrated HEPA/FFU ceilings — it ships flat, assembles fast on your Dammam or Jubail site, and can be reconfigured later without demolishing the building.

Shipping to Dammam Through King Abdul Aziz Port

King Abdul Aziz Port in Dammam is the natural gateway for cleanroom equipment entering the Eastern Province, and it is the route we build our logistics around. We consolidate panels, doors, windows, FFUs, HVAC components and pass boxes into sea containers in Pakistan and ship under CIF or DAP Incoterms, so you have a clear landed cost before anything leaves the factory.

Typical project lead time runs roughly 4 to 8 weeks for design and fabrication, depending on classification and room size, plus ocean transit and customs clearance at Dammam. Because Pakistan and Saudi Arabia sit on relatively short Arabian Sea shipping lanes, transit times into King Abdul Aziz Port are shorter than equivalent shipments from East Asia or Europe — a meaningful advantage when a production schedule is fixed.

  • Factory consolidation and container loading in Pakistan
  • Sea freight to King Abdul Aziz Port, Dammam (CIF or DAP)
  • Optional installation and commissioning supervision at extra cost
  • Documentation pack prepared for customs and SFDA submission

Built to Meet SFDA and International Standards

In Saudi Arabia the relevant regulator is the Saudi Food and Drug Authority (SFDA), and any cleanroom serving pharmaceutical, biotech or medical-device production in the Eastern Province must stand up to its expectations. We are precise about our role here: Pak Gusu does not hold an SFDA approval and we will never claim one. Instead, we design and document cleanrooms that are validation-ready for SFDA — compliant with the standards SFDA references and supported through your own submission.

Our reference framework includes ISO 14644 for classification and monitoring (ISO 5–8 covers most pharma and healthcare needs), EU-GMP Annex 1 for sterile manufacturing, ISO 13485 for medical-device quality systems, plus WHO and GSO guidance applied across the GCC. Every project ships with the technical and validation documentation your quality team and consultants need to demonstrate compliance to the authority.

  • Classification and airflow design to ISO 14644
  • Grade A/B/C/D zoning to EU-GMP Annex 1 for sterile processes
  • As-built drawings, airflow schemes and validation-support documents
  • We support your SFDA submission — we do not submit on your behalf

From Enquiry to Commissioned Cleanroom

A Dammam project usually starts with your URS or a simple description of the process, target classification and available floor area. From there we move through a defined sequence so there are no surprises on site.

First, our engineers produce a concept layout, airflow strategy and budgetary quote. Once the design is fixed, we fabricate the modular envelope and air-handling package in Pakistan, run factory checks, then consolidate and ship to King Abdul Aziz Port. On arrival, your contractor can assemble the system, or our supervisors can travel to oversee installation and commissioning for an additional fee.

  • Design: layout, classification and airflow concept agreed against your URS
  • Manufacture: panels, doors, FFU ceilings and HVAC built and tested in-factory
  • Ship: containerised delivery to Dammam under CIF or DAP
  • Install: self-build with our drawings, or supervised installation at extra cost
  • Validate: documentation provided so your team can complete IQ/OQ/PQ and SFDA filing

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Answers

Frequently Asked Questions

Common questions about cleanrooms, standards, cost and how Pak Gusu supplies and installs across the GCC.

Does Pak Gusu have an office in Dammam?

No. Pak Gusu manufactures cleanrooms in Pakistan and exports them to Dammam and the Eastern Province. We do not maintain a Saudi office or local licence. We ship validation-ready modular cleanrooms through King Abdul Aziz Port and can send engineers for on-site installation and commissioning supervision at additional cost.

Are your cleanrooms approved by the SFDA?

We do not hold SFDA approval and never claim to. Our cleanrooms are designed to meet the standards SFDA references — ISO 14644 and EU-GMP Annex 1 — and ship with validation-ready documentation. SFDA approval applies to your facility and submission, which we support by supplying the technical evidence your team and consultants need.

How are cleanrooms delivered to the Eastern Province?

We consolidate panels, doors, FFUs and HVAC into sea containers in Pakistan and ship under CIF or DAP Incoterms to King Abdul Aziz Port in Dammam. From the port your contractor handles inland transport to Dammam, Jubail, Khobar or Dhahran. Optional installation supervision by our engineers is available at extra cost.

What is the typical lead time for a Dammam cleanroom project?

Design and fabrication usually take about 4 to 8 weeks depending on classification and size, followed by sea transit and customs clearance at King Abdul Aziz Port. Because Pakistan sits on short Arabian Sea routes to Saudi Arabia, transit into Dammam is typically faster than comparable shipments from East Asia or Europe.

Which industries in Dammam do you build cleanrooms for?

We serve the Eastern Province's main sectors: pharmaceutical and sterile-fill suites to EU-GMP Annex 1, medical-device assembly aligned with ISO 13485, electronics and semiconductor environments with ESD finishes, and QC and microbiology laboratories. Each cleanroom is engineered to the required ISO 14644 class, from ISO 5 through ISO 8, for the specific process.

Can you build to EU-GMP Annex 1 grades for sterile production?

Yes. We design sterile and aseptic suites to EU-GMP Annex 1, mapping Grade A and B to ISO 5, Grade C to ISO 7 and Grade D to ISO 8. Layouts include proper zoning, airlocks and pressure cascades, with airflow schemes and as-built documentation prepared so your team can validate the rooms and support an SFDA filing.

Cleanrooms supplied & installed across the GCC

Manufactured in Pakistan with GUSU (China) technology · shipped to Jebel Ali, Dammam & Hamad (CIF/DAP) · installation available across the Gulf.

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