Digital Quality & Operations Built for TGA-Audited Manufacturers
A structured 5-day paid diagnostic that stabilises your SharePoint workflows across CAPA, deviations, change control, and approvals.
When the Factory Floor Runs Smooth
BUT SharePoint Doesn’t
01
Traceability Breakdowns
CAPA tasks go missing. Approvals stall. Managers lose visibility.
02
Document Overload
SOPs, batch docs, deviations scattered across sites. Audit chaos.
03
Multi-Brand Complexity
Dozens of SKUs and client QC demands with no unified workflow model.
SharePoint Isn’t the Problem,
The Architecture Is
Regulated environments outgrow SharePoint’s default settings fast.
When workflows, sites, lists, roles, and permissions evolve without a deliberate architecture, you get:
Approval bottlenecks
Unclear responsibilities
Duplicate records
Audits requiring last-minute reconciliation
This is where most contract manufacturers hit the wall — and where the 5-Day Digital Quality Ops Reset begins.
WHAT YOU GET IN 5 DAYS
The 5-Day Digital Quality Ops Reset (Paid Diagnostic)
Day 1 - Discovery Session
What happens:
We sit down with your team and uncover the pain points, priorities, bottlenecks, compliance risks, and daily operational realities.
Day 2 - Deep-Dive Research
What happens:
We audit your Microsoft 365, SharePoint, Teams, OneDrive, permissions, structure, and integration points.
Outcome:
Your “digital truth map” — what’s broken, what’s missing, and what’s worth fixing.
Day 3 - UX & Architecture Design
What happens:
We design the cleanest, simplest, most scalable way to fix your system — without overbuilding anything.
Outcome:
The structure your team will actually use.
Day 4 - Documentation (The Blueprint Build)
What happens:
We document recommended fixes, workflows, permissions, data paths, MVP scope, and future-phase opportunities.
Outcome:
Your roadmap to digital sanity.
DAy 5 - Peer Review & Prioritisation
What happens:
We sanity-check everything, validate with your team, and lock in the priority list.
Outcome:
A confident, clear, step-by-step execution plan.
Why This Reset Works for TGA-Audited Manufacturers
Built for GMP workflows
Designed for multi-brand SKUs
CAPA / deviation / change control prioritised
Replaces Excel-based tracking
Reduces audit prep dramatically
Clarifies ownership across QC + Ops + IT
How Workflows Change After the Reset
When a GMP Facility Fixes Its Digital Backbone
An Australian manufacturer went from:
14 days of audit prep → 2 hours
11 Excel trackers → zero
Multi-step approvals → one streamlined flow
Team confusion → clear operational visibility
What You’ll Walk Away With
