Compliance Gets Expensive When You Leave It Too Late
Product compliance requirements vary by market and by product type. Getting them wrong means failed tests, forced redesigns, and delayed launches. Getting them right, early, as part of the design process, saves significant time and money.
Pro-Dev has managed compliance for consumer products, medical devices, and industrial equipment across New Zealand, Australia, the United States, and Europe. We know what the requirements are, how to plan for them, and how to get your product approved without it derailing your timeline.
What We Deliver
Compliance Planning
Identifying applicable standards at the design stage, before they become costly to retrofit
Standards Navigation
NZ (AS/NZS), AU (RCM), USA (FCC, UL, CPSC), EU (CE, RoHS), and global markets
Test Lab Coordination
We work with SGS, ITS, and other internationally accredited labs
Compliance Documentation
All the paperwork your product needs to be legally sold in your target markets, prepared and managed by us
Labelling Requirements
Required markings designed into packaging and product from the start
Medical Device Compliance
TGA (AU), FDA (USA), Medsafe (NZ)
Why Plan Compliance Early
Most compliance problems are design problems that were not caught early enough. Compliance requirements affect material choices, dimensions, electrical ratings, and labelling. When these requirements are identified at the design stage, meeting them is straightforward and cost-effective. When they are discovered after tooling has been cut, fixing them is expensive, time-consuming, and sometimes means starting significant parts of the design again.