O ORPAON

Personal Care & Pharma

With data integrity as the bottom line, covering facility monitoring and laboratory informatization for high-standard audit scenarios.

Industry pain points

  • GMP compliance and data integrity are hard gates in audits — incomplete records become findings.
  • Facility systems (HVAC / water / gas / electricity) directly affect production quality.
  • Laboratory and R&D data are scattered; formula and batch management depends on manual work.

Our solution

  • SCADA and FMCS facility monitoring: an integrated production and facility monitoring platform — purified water treatment, air handling units, centralized supervision of utilities and alarm governance, with multilingual delivery experience for foreign-invested factories.
  • Production informatization: material call system (closed loop of material call → delivery → line-side confirmation), single-tank / single-line OEE, data collection and batch traceability.
  • LIMS and R&D informatization: laboratory information management system solutions for pharmaceutical R&D laboratories (PRD-level design capability), formula and batch data management.
  • Data integrity engineering: the permissions / roles / audit trio as standard, full-element timestamps for man, machine, material, method and environment — supporting foreign customers' high-standard audits.

Representative projects

  • A health products company: long-term combined delivery of SCADA configuration, material call, data collection and single-tank OEE.
  • A pharmaceutical research institution: LIMS and FMCS solution design.
  • A medical logistics company: logistics traceability and purified water treatment monitoring.
  • A personal care major's system: PLC program standardization across multiple production lines.

Capability extensions

  • Carbon management and green factory applications, digital twin workshops, SPC quality analysis.

Buying scenarios and conversion paths

Target roles

  • · QA/QC lead
  • · Engineering lead
  • · EHS lead

Trigger events

  • · GMP / data integrity inspection remediation
  • · Facility system failures affecting production
  • · Preparation for foreign customers' high-standard audits

Product pilot path

When your product requirements are already clear: start with a 15-minute demo and a small-scale pilot — you can begin with data collection and report automation.

Book a Product Demo

Full project path

When you only have an industry-level question: start with an on-site diagnosis and a phased proposal. SCADA, FMCS facility monitoring, material call system and LIMS support, built in phases.

Request an On-site Diagnosis

GMP compliance and facility stability — start with an on-site diagnosis.

Tell us about your industry and site conditions to get a diagnosis and phased solution proposal.

Request an On-site Diagnosis