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YanMaoPackaging Systems

Gentle, validated and serialization-ready case packing

Diagnostics, medical devices and pharmaceuticals demand gentle handling, documented validation and traceability. Our pharma vertical delivers anti-static product handling, 21 CFR Part 11 friendly controls and complete IQ/OQ documentation.

21 CFR Part 11 audit-ready controlsGMP and IQ/OQ validation documentationAnti-static, low-particle handlingSerialization-ready interfaces

Problem / Solution

The real production problems — and the engineering answers

The problem

Diagnostic strips, vials and devices are fragile and static-sensitive.

Our answer

Anti-static end-of-arm tooling, soft-servo compliance and low-impact transfer paths keep rejection rates near zero.

The problem

Regulatory audits require proof — materials, validation, change control.

Our answer

Complete IQ/OQ packages, material certificates and documented FAT/SAT reports are standard deliverables for every pharma line.

The problem

Serialization and aggregation must integrate without breaking the line speed.

Our answer

Camera-verified tracking and handshakes to serialization software are engineered in at the design stage, not bolted on later.

IQ/OQ complete

Validation package

near zero

Rejection rate

ready

Serialization

Reference Installations

Pharma & Medical plants we've already served

0+

Lines installed worldwide

0

Export markets served

0+

National invention patents

Ready to engineer your line?

Engineer your Pharma & Medical line with us

Tell us about your product, materials and regulatory requirements — we'll reply with the right architecture and relevant references within one business day.