ISO cleanroom classifications and GMP requirements apply to facilities and operations; a panel contributes to compliance but is not independently “GMP certified” by default.
Key Points
- Define the governing country, code, cleanroom class and user requirements.
- Request test reports or declarations for the exact panel construction where needed.
- Review cleanability, shedding, joints, penetrations and maintenance access.
- Keep approved drawings, material records and inspection documents in the project file.
Quick Reference
| Decision Stage | Recommended Action | Output |
|---|---|---|
| Define | Record the process, room conditions and governing requirements | User requirement or project brief |
| Compare | Review complete panel constructions and interfaces | Shortlisted technical options |
| Verify | Check drawings, samples and applicable documents | Approved quotation and submittal |
| Deliver | Coordinate packing, installation and inspection | Traceable project records |
How AILV Uses This Information
AILV reviews the application, environment, dimensions, interfaces, documentation needs and destination before confirming a panel construction or project scope. Website guidance does not replace approved drawings, specifications or local engineering review.
Frequently Asked Questions
Does ISO 14644 certify a panel?
ISO 14644 primarily addresses cleanroom classification and related controls; it is not a universal product certificate for a wall panel.
What should I ask a supplier for?
Ask for documents named in the specification, such as material data, drawings, applicable test reports, inspection records and packing lists.
Discuss Your Cleanroom Panel Inquiry
Send the application, room dimensions, target environmental conditions, preferred panel construction and project schedule to albert@ailvtech.com. Phone/WhatsApp: +8617300630130.