What are the opening hours?

Monday 7:30am - 5pm Tuesday 7:30am - 5pm Wednesday 7:30am - 5pm Thursday 7:30am - 5pm Friday 7:30am - 5pm

CPL Group

Home
New Zealand
Kaiwaka
CPL Group

We manufacture a range of customizable PVC screening solutions.

25/08/2026

A distribution centre in Townsville and one in Hobart aren't managing the same heat load, and a curtain spec that works in one climate zone isn't automatically right for the other.

We looked at why more Australian DCs are choosing modular PVC curtains over permanent partition walls, including the real approval-and-downtime gap between the two options.

https://cplgroup.com/au/blog/distribution-centres-choosing-modular-pvc-curtains-in-australia/

19/08/2026

Loading docks account for roughly a quarter of all warehouse accidents. Door and boundary openings account for 20–35% of cooling energy loss in busy cold storage facilities.

Different stats, same root cause: an unmarked zone boundary that's costing you twice.

We put together the case for treating zoning as one problem instead of three.

https://cplgroup.com/blog/real-cost-warehouse-zoning-solutions/

11/08/2026

A classification certificate isn't a Contamination Control Strategy.

Annex 1 wants to see the system behind the number: facility design, monitoring, and procedure working as one plan, not three separate ones.

Our new article breaks down what changed under the 2022 Annex 1 revision, and what it means for cleanroom design specifically.

🔍 See how your sites compare against the EU checklist: https://cplgroup.com/eu/blog/clean-room-solutions-eu-pharma-lab/

06/08/2026

Passed its first classification. Never checked since.

That's the pattern behind a lot of Medsafe findings: cleanrooms that were compliant on day one and drifted quietly from there.

Our new article looks at where NZ cleanrooms lose ground, and what keeps a classification holding up over time.

👉 Send this to whoever's due for a cleanroom review: see link in comments.

04/08/2026

A clean swab result doesn't mean a compliant cleanroom anymore.

TGA auditors want to see the system behind the number: classification, monitoring trends, and a pressure cascade that was designed on purpose, not fixed after the fact.

Our new article breaks down what's changed in TGA cleanroom expectations, and where builds fall short before the room is ever classified.

📥 Get the AU cleanroom checklist and see how your facility measures up: https://cplgroup.com/au/blog/clean-room-solutions-australia-pharma-lab/

28/07/2026

Not a global rulebook. Four regulators reading from the same technical page.

TGA, Medsafe, MHRA and the EU's Annex 1 all describe cleanroom compliance differently on paper, but they're drawing from the same ISO 14644 foundation.

See how AU, NZ, EU and UK cleanroom rules connect, and what that means if you're building across more than one region.

Get the full regional breakdown and our Global Cleanroom Readiness Guide
🔗 in the comments.

23/07/2026

One set of regulations. Multiple inspectors.

EU GDP provides the framework, but every member state expects facilities to demonstrate compliance during inspection.

If you're operating across multiple countries, consistent facility design and documented validation make audits far easier to manage.

Our latest article explains what EU inspectors look for in temperature-controlled pharmaceutical and laboratory storage.

Compare your facility against current GDP and GMP requirements before your next audit.

📥 Download the checklist: see link in comments!

21/07/2026

Is your cold storage ready for a Medsafe inspection?

Many pharmaceutical and laboratory facilities are still operating cold rooms that have never been fully mapped or validated. That's often where compliance issues begin.

Our latest article looks at the most common cold chain risks facing New Zealand facilities and what Medsafe inspectors expect to see.

Free Resource: A practical checklist to review your cold storage before your next inspection.

📥 Download the checklist: see link in comments

17/07/2026

Your cold room can hold temperature and still fail a TGA inspection.

Temperature logs are only part of the picture. Auditors also look at how the facility was built, validated and maintained. Poor insulation, thermal bridging, damaged door seals and incomplete validation can all put compliance at risk.

Review your facility against the same areas inspectors assess before your next audit.

Our latest article explains what TGA and PIC/S expect from pharmaceutical and laboratory cold storage, and where facilities commonly fall short.

Get your Free Resource: TGA & PIC/S Cold Chain Compliance Checklist for Pharmaceutical & Laboratory Facilities

See link in comments!

15/07/2026

Different regulators. The same cold chain fundamentals.

Whether you're working under TGA, Medsafe, EU GDP or MHRA requirements, the principles remain the same. Validated infrastructure, temperature mapping, continuous monitoring and documented quality systems all play a critical role in compliance.

Compare international requirements and strengthen your compliance strategy across every site.

Our latest resource compares the major regional requirements and shows what pharmaceutical and laboratory facilities should have in place.

🔗 See link in comments

Address

1800 SH1
Kaiwaka
0573

Opening Hours

Monday	7:30am - 5pm
Tuesday	7:30am - 5pm
Wednesday	7:30am - 5pm
Thursday	7:30am - 5pm
Friday	7:30am - 5pm

Website

https://www.cplgroup.com/

Alerts

Be the first to know and let us send you an email when CPL Group posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Business

Send a message to CPL Group:

Want your business to be the top-listed Equipment Service in Kaiwaka?