Industry1 min read

Flexo Printing for Pharmaceutical Packaging: GMP Compliance and Validation

Guide to flexographic printing for pharmaceutical applications covering GMP compliance, serialization, low-migration inks, and IQ/OQ/PQ validation procedures.

L
LISHG Editorial
December 16, 2025
Flexo Printing for Pharmaceutical Packaging: GMP Compliance and Validation
Article overview

Guide to flexographic printing for pharmaceutical applications covering GMP compliance, serialization, low-migration inks, and IQ/OQ/PQ validation procedures.

Flexo Printing for Pharmaceutical Packaging: GMP Compliance and ValidationIndustryguideLISHG Machineryflexographic printing machine
Article Content
In-depth analysis, specifications and editorial commentary

Pharmaceutical Flexo Requirements

Pharmaceutical packaging demands a higher quality assurance level than any other flexo application. Patient safety, regulatory compliance, and zero-defect standards require specialized machine configurations and validation procedures.

GMP Compliance Features

  • IQ/OQ/PQ validation documentation package included
  • 21 CFR Part 11 compliant electronic records and audit trail
  • Calibrated instruments with traceable certificates
  • Cleanable stainless steel surfaces in product contact zones

Serialization and Track-and-Trace

100% vision inspection system verifies 2D DataMatrix codes and serial numbers at full production speed. System integrates with pharma track-and-trace networks (DSCSA, EU FMD compliance). Reject mechanisms automatically remove unverified units.

Ink Selection

Low-migration UV inks formulated to Nestlé Guidance and Swiss Ordinance standards prevent migration to drug products. LISHG works with certified ink suppliers to ensure regulatory compliance for each customer's specific pharmaceutical application.