Quality
QUALITY COMMITMENT
At Qpharma, quality is at the core of everything we do. We are committed to delivering products that meet or exceed all legislative requirements, Good Manufacturing Practice (GMP) standards, and customer expectations. Our robust Quality Management System (QMS) is designed to ensure the highest levels of product quality, safety, and efficacy across all stages of manufacturing.
We are licensed by the Australian Pesticides and Veterinary Medicines Authority (APVMA) and certified to ISO 22716 for Cosmetics Good Manufacturing Practices. Our facilities and processes are regularly audited to maintain compliance with these standards.
Our Capabilities
Qpharma manufactures APVMA-registered and non-registered products for Animals at an APVMA approved site. It also manufactures products certified under ISO 22716 Cosmetics at an ISO certified facility.
Our manufacturing processes include:
- Quality assurance of raw materials and packaging
- Blending, dry milling, granulation, and mixing
- Filling, packaging, labelling, blister packaging, and tableting
- Physical testing, storage, and release for supply.
Quality System Framework
Our Quality System is built on internationally recognized principles and includes:
- Standard Operating Procedures (SOPs) and Work Instructions (WIs)
- Non-Conformance (NCF) and Change Control (CC) management
- Corrective and Preventative Actions (CAPA)
- Risk assessments and process validations
- Equipment qualification and calibration
- Full batch traceability via our integrated MRP system
- Customer complaint handling and adverse reaction reporting
- Ongoing Continuous Improvement initiatives