SOLVE⁴ · EST. 2020 · VANCOUVER, BC / CANADA & UNITED STATES
Solve⁴ Solutions Inc
Solve4  /  04 / Consulting

Performance, quality inspection & GMP readiness.

Practical TPM, Kaizen, quality inspection, supplier audit, SOP, CAPA, and GMP consulting for operators that need cleaner production systems, fewer preventable failures, and documentation that survives real-world use.

Operational discipline

We make the work visible, measurable, and repeatable.

Solve4 works with production, packaging, cannabis-adjacent, food, vape, and regulated-product teams that need practical improvement, not a binder full of theory. The focus is simple: stabilize the process, inspect the right points, document the standard, and improve the line without slowing the business down.
01

Performance systems

TPM, Kaizen, OEE reviews, downtime tracking, changeover reduction, standard work, and visual management for production teams that need better daily control.

  • TPM audits and maintenance routines
  • Kaizen event planning and facilitation
  • OEE, downtime, waste, and bottleneck reviews
02

Quality inspection

Incoming, in-process, pre-shipment, and supplier inspection workflows for products, packaging, equipment, and regulated components before issues reach the customer.

  • Inspection checklists and sampling plans
  • Supplier and factory audit support
  • Non-conformance and corrective action tracking
03

GMP readiness

Gap assessments, SOPs, batch records, sanitation workflows, training records, CAPA, and documentation systems built for food, cannabis-adjacent, vape, and production environments.

  • GMP gap assessments
  • SOP and record template development
  • Training, CAPA, and audit preparation
How engagements work

Start with the floor, then build the system.

01 · Observe Walk the process

Map the real workflow, inspection points, bottlenecks, handoffs, downtime, and documentation gaps.

02 · Stabilize Fix the obvious failure points

Prioritize practical changes: standard work, preventative maintenance, incoming checks, and changeover discipline.

03 · Document Build usable SOPs and records

Create forms, checklists, logs, CAPA workflows, and training documents that operators can actually follow.

04 · Improve Track and tighten

Set the cadence for metrics, audits, corrective actions, and continuous improvement so gains do not fade.

Need help with performance, inspection, or GMP readiness?

Send the process, product type, current pain points, and any inspection or audit requirements. We’ll come back with a practical consulting scope.