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Zetron Technology at CPHI South East Asia 2026: Precision Cleanroom Particle Monitoring for Pharmaceutical Manufacturing

2026-07-10

The pharmaceutical manufacturing world gathers in Bangkok this week, and Zetron Technology is right in the middle of it. From July 8 to 10, 2026, we are exhibiting at CPHI South East Asia 2026, the region’s leading event for pharmaceutical ingredients, manufacturing, and quality control. You’ll find us at Booth S31 inside the Queen Sirikit National Convention Center (QSNCC). Stop by to see our cleanroom particle counters in action and talk with the engineers who build them.

Zetron's instruments are designed for a specific purpose. They help keep pharmaceutical cleanrooms clean and compliant. In sterile drug production, the number of airborne dust particles in a room is a direct measure of contamination risk and a regulated one. Our particle counters equip QC teams with the rapid, traceable data they need to verify that a Grade A, B, C, or D area functions correctly.

The Event at a Glance

Event	CPHI South East Asia 2026
Dates	July 8–10, 2026
Venue	Queen Sirikit National Convention Center (QSNCC), Bangkok, Thailand
Zetron Booth	S31
On Display	B110-PRO, B330, H630, and R310P cleanroom particle counters

Why Cleanroom Particle Monitoring Matters in Pharma?

Contamination control is not an option in sterile manufacturing. One particle in the air can ruin a batch of injectables, delay a product release or result in a regulatory finding. Standards like ISO 14644-1 and GMP Annex 1 have been developed because particle counts are one of the most apparent and objective indicators of cleanroom performance.

That’s the work Zetron’s instruments are built for: cleanroom qualification, static and dynamic environmental validation, plant acceptance testing, and routine daily monitoring. Our counters are made for the people who take contamination control seriously QC teams, validation specialists, and production engineers who need numbers that hold up in an audit.

Zetron Technology at CPHI South East Asia 2026: Precision Cleanroom Particle Monitoring for Pharmaceutical Manufacturing 1

The Particle Counters We're Showcasing at Booth S31

We're bringing four cleanroom particle counters, each built for a different point in the workflow. The B110-PRO is a GMP-ready handheld with FDA 21 CFR Part 11 records for regulated checks. The B330 is the high-capacity unit for fast cleanroom qualification. The H630 is a lightweight handheld for daily spot checks, and the R310P is an online sensor for round-the-clock Grade A/B monitoring. The quick comparison below shows how they line up.

Quick Comparison

Feature	B110-PRO	B330	H630	R310P
Type	Handheld, GMP	Portable, high-capacity	Handheld	Online / fixed
Flow rate	28.3 L/min	28.3 L/min	2.83 L/min	28.3 L/min (built-in pump)
Size channels	8 (0.1–5.0 µm)	8 (0.3–10.0 µm)	6 (0.3–5.0 µm)	0.3 / 0.5 / 5.0 µm
Housing	316L stainless steel	Stainless steel	ABS, lightweight	Stainless steel
Data storage	1M+ records	1M records	USB-rechargeable, 8h+	Continuous / networked
Best for	GMP handheld checks	Cleanroom qualification	Daily spot checks	24/7 Grade A/B monitoring

Where These Instruments Fit — From Sterile Suites to QC Labs

Particle counting shows up at nearly every stage of pharmaceutical production. Here’s where our customers put these instruments to work every day.

Pharmaceutical Setting	Where the counters are used
Pharmaceuticals & Biomedicine	Sterile drug workshops, injections, lyophilized products, eye drops, infusions; daily Grade A/B/C/D monitoring; static & dynamic validation; plant acceptance testing
Biopharma, Vaccines & Cell Therapy	Cell culture rooms, virus-handling isolators, fermentation prep, sterile testing and microbial limit rooms
Medical Device Manufacturing	Clean assembly of syringes, infusion sets, implantable stents and sterile surgical consumables
Pharmaceutical QC Laboratories	Sterile testing rooms, positive-control rooms, weighing and sampling negative-pressure areas
Hospital Clean Areas	Clean operating rooms, CSSD sterile storage, PIVAS dispensing, neonatal sterile wards

In addition to pharma, the same equipment is used in semiconductor and electronics cleanrooms, for sterile food and cosmetics manufacturing, and for third-party clean room testing labs in any location where clean conditions must be verified, and not assumed.

Zetron Technology at CPHI South East Asia 2026: Precision Cleanroom Particle Monitoring for Pharmaceutical Manufacturing 2

Beyond Particle Counters: A Complete Cleanroom Toolkit

Particle counting is where many conversations start, but Zetron supplies the wider set of instruments a pharmaceutical cleanroom depends on.

Our Filter Integrity Testers verify sterile filter cartridges and membranes by bubble point, diffusion flow, and water intrusion supporting PUPSIT and post-use testing under GMP Annex 1 and USP <1207>. Our Glove Integrity Testers detect micron-level leaks in isolator and RABS gloves before and after each batch, protecting both product sterility and operators. Add TOC analyzers, biological air samplers, HEPA filter testers, and online FMS systems, and a facility can source its entire cleanroom monitoring stack from a single partner.

This one-source solution reduces time, service and ensures quality uniformity throughout a site. More than 100 patents and 20 years of manufacturing experience support Zetron products that are certified CE, ATEX and ISO, and meet GMP, FDA 21 CFR Part 11 and pharmacopoeia standards.

What You Get When You Visit Us

Drop by Booth S31 and you can:

• See the B110-PRO, B330, H630, and R310P running live

• Talk through your specific cleanroom or GMP monitoring challenge with our engineers

• Explore filter and glove integrity testing for sterile production lines

• Learn about OEM/ODM options plus our 12-month warranty and lifetime maintenance

Let’s Connect in Bangkok

CPHI South East Asia 2026 brings the region’s pharmaceutical community together under one roof, and we’re glad to be part of it. Come see our GMP-ready cleanroom particle counters in action, ask the hard questions about contamination control, and let’s explore what we can build together.

Visit Zetron Technology at Booth S31 and explore our full pharmaceutical cleanroom range at www.bjzetron.com.

Our Solutions: Sterility Assured, Contamination Controlled

Zetron's instruments are only the starting point what we actually deliver are complete solutions to the problems that carry real regulatory weight: sterility assurance, contamination control, microbial testing, and pharmaceutical quality. Instead of selling standalone devices, we help pharmaceutical facilities build a monitoring approach that holds up under GMP audit, from cleanroom acceptance to everyday production.

It comes together in two connected layers:

1. Cleanroom Monitoring Solutions

Built for pharmaceutical factories and laboratories, these keep watch over the entire cleanroom environment. They confirm that cleanliness levels hold, track the air and conditions inside the room, and give QC teams continuous proof that a controlled space is staying controlled.

→ Cleanroom Monitoring Equipments

2. Pharmaceutical Analytical Solutions

This is where sterility gets verified at the point of production. Used across pharma factories and labs, these instruments catch problems during drug manufacturing and confirm the absence of microbial contamination in aseptic processes. The range brings together the Filter Integrity Tester, TOC Analyzer, and Glove Integrity Tester, each one part of a larger sterility-assurance solution.

→ Pharmaceutical Analytic Instruments

Together they do one job: monitor the environment, verify the process, and document it all to GMP standards. That's the Zetron solution and it's exactly what our team will walk you through at Booth S31.

Zetron Technology at CPHI South East Asia 2026: Precision Cleanroom Particle Monitoring for Pharmaceutical Manufacturing 3

Frequently Asked Questions

1. What does Zetron make for pharmaceutical cleanrooms?

Handheld, portable and online cleanroom particle counters, filter integrity testers, glove integrity testers, TOC analyzers, biological air samplers and complete FMS systems for GMP regulated cleanrooms.

2. Where can I find Zetron at CPHI South East Asia 2026?

We’re at Booth S31 at the Queen Sirikit National Convention Center (QSNCC) in Bangkok, from July 8 to 10, 2026.

3. Are the particle counters GMP and ISO compliant?

Yes. They comply with ISO 14644-1, ISO 21501-4, GMP (including Annex 1) and FDA 21 CFR Part 11 for electronic records and signatures, depending on the model.

4. Can these instruments be used outside pharma?

Yes. The same counters serve semiconductor, electronics, food, cosmetics, aerospace, and third-party testing cleanrooms wherever strict cleanliness levels apply.