Melbourne/ Sydney/ Brisbane
+61 3 8761 9264 contact@australiaquality.com.au
Australia Quality Group Quality · Compliance · Regulatory Book a consultationContact
Consulting · Training · Regulatory support

Compliance that
holds up under
audit.

We build ISO 9001, GMP, HACCP and TGA-ready quality systems that regulators accept and operators actually use — designed around how your business already runs.

ISO 9001GMPISO 22716HACCPTGA
Automated production line with an engineer monitoring the process
01 — What we do

Four practices, one system of record

All services
01 Quality management systems ISO 9001 and integrated systems built to your process, not a template library. 02 GMP & TGA compliance Pharmaceutical, cosmetic and device manufacturing readiness through to licence approval. 03 Regulatory services Product dossiers, listings and agency correspondence handled end to end. 04 Operations strategic review Lean diagnostics that connect compliance work to throughput and cost.
02 — Why Australia Quality Group

Quality systems designed around the way your business works.

Operations Strategic Review: two engineers in hard hats reviewing an operational performance dashboard on a factory floor

Meeting a regulatory requirement and running a workable business are the same problem, not two. We design quality systems that satisfy the standard and still fit the way work actually moves through your site — so procedures are used rather than filed.

Practical systems

Documentation written for the people who use it, sized to the business rather than the standard's page count.

Audit readiness

Evidence, records and responsibilities in place before an inspection is scheduled, not after it is announced.

Continuous improvement

The same system used for compliance becomes the one you use to find waste and lift performance.

03 — Training courses

Courses that build capability inside your team.

View the full course list →
Online course ISO 9001 Awareness Training An introduction to the quality management standard — what it asks for, and what an auditor looks for in everyday practice. View course → Online course Internal Audit Training Plan, run and report internal audits against ISO 19011 so they surface real findings rather than paperwork. View course → Online course ISO 22716 Cosmetic GMP Training 2026 The key good manufacturing practice requirements for cosmetic production, packing and in-process control. View course → Online course Operations Strategic Review (OSR) Value-stream mapping and the seven wastes, applied to connect operations work to throughput, lead time and cost. View course → Online course Pharmaceutical GMP GMP for pharmaceutical manufacture — documentation, cleaning and sanitisation, and the quality system behind PIC/S and TGA expectations. View course → Online course Quality Risk Assessment Training Risk assessment as a preventive tool — FMEA and hazard analysis in line with ICH Q9, ready to apply to real decisions. View course →

Every course is delivered online, so a team can be trained without pulling everyone into the same room on the same day.

04 — Expertise

Regulated industries, understood from the inside.

Work spans health products, food and general manufacturing, including businesses that import or wholesale rather than manufacture.

Laboratory corridor with analysts working at the bench
05 — Success stories

Compliance work that shows up in the numbers.

Read the success stories →
Medical device Zero major findings for first TGA inspection A first TGA inspection completed with no major findings recorded.
Cosmetics Streamlined documentation system for a cosmetic manufacturer An ISO 22716 documentation set merged and rewritten, removing roughly a fifth of the pages.
Printing Make ready time reduction at a printing company Make-ready time cut by a third and efficiency lifted 53% within the first three months.
Pharmaceutical Inventory reduction at a pharmaceutical A stock holding study found a tenth of inventory could be released while staying inside benchmark.
Laboratory Equipment utilization gain at a Laboratory HPLC utilisation lifted inside two weeks, with reporting time down from 210 minutes to 60.
Pharmaceutical Lead time reduction at a pharmaceutical Lead time reduced across three years as raw-material availability rose into the high 90s.
06 — Who you work with

Experienced guidance when the details matter.

Consulting is led by Kok Yin Loke, Principal Consultant, working directly with your team rather than at a distance.

Kok Yin Loke — Principal Consultant

Preparing for an audit, certification or regulatory inspection?

Start with a conversation about where your business is today and what needs to happen next.

Book a consultation
Telephone
+61 3 8761 9264
Office
Waterman Business Centres
Suite 064, 44 Lakeview Drive
Scoresby VIC 3179