Discuss a programme with Nagoya.
Tell us what you are planning. We execute a confidentiality agreement before any drawing, specification or commercial detail is exchanged.
Nagoya Plastic Industry Sdn. Bhd.
Plot 89, 90 & 91, Jalan Aman 2, Kawasan Perusahaan Taman Makmur, Sungai Seluang, 09600 Lunas, Kedah Darul Aman, Malaysia
What happens next
We agree and sign a confidentiality agreement.
You share drawings, volumes and requirements.
We assess capability and capacity against your specification.
Site audit or visit, at any stage you choose.
How we work with you.
Confidentiality & ownership
Confidentiality agreement first. Tooling ownership, design rights and data handling are defined in writing before work begins.
Continuity & supplier controls
All production runs on our Lunas campus, with documented continuity planning, tooling protection and an inventory strategy agreed with you. Sub-tier suppliers are qualified, monitored and dual-sourced where a programme’s risk profile requires it.
See our Lunas campus for yourself.
Supplier audits and site visits are welcome at any stage, from first contact onwards. During your visit you can review our current certificates, validation and calibration records, and quality agreement templates. Our campus in Lunas, Kedah is within reach of the Penang and Kulim manufacturing clusters.
A few useful starting questions.
Can I discuss an early-stage project?
Yes. Begin with the intended application, development stage and manufacturing questions. We agree a confidentiality agreement before you share drawings, specifications or commercial details.
What if I already have a mould?
Mention that you are considering a tool transfer. Tool information, part drawings, material, current machine requirements and available production records will help the team understand the review needed.
Can we discuss finishing and assembly together?
Yes. Include the coating, printing, marking or assembly requirements in your enquiry, along with the inspection and packaging needs of the finished component.
What should a medical enquiry include?
Explain the intended application, materials, cleanroom requirements, expected volume and any validation or traceability requirements. The team can then discuss the applicable scope.