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QualityShield+TM

Consistent and reliable complementary medicines to the highest quality standards.

Our Lipa Total QualityShield+™

Our Lipa QualityShield+™ Quality Control process, allows us to be in strict control of total quality management, from the initial product design, all the way through to launch and on-going at every stage of the continual production process.

We take pride in our commitment to Quality and the provision of our own, market leading, fully internal scientific chemical, microbiological and internal validation and testing process and global regulatory compliance team.

Lipa Total QualityShield+™ provides our customers the reassurance of the highest product Quality and Compliance, critical to ensuring the products success in the market.

Product Design

Concept development, evidence consolidation, indication, pharmacology and scientific evidence review, ingredient safety and high-level compliance review

NPD Formulation

Detailed review of formulation for ingredient compliance and product feasibility.

R&D assessment and development of product trials. QC evaluation of required testing.

Ingredient selection

Ingredients sourced from reputable and validated suppliers.

Regulatory pre-assessment to determine ingredient quality and compliance.

Internal QA

Rigorous internal quality evaluation and re-evaluation of full ingredient dossier & vendor qualifications. Full internal scientific review of chemical and microbiological attributes and thorough evaluation of supplier, including manufacturing processes and compliance review.

Final Product Assurance

Pending the successful outcome of Internal QA, all ingredients receive final sign-off from our Quality Assurance team with confirmation that production can commence.

Our strict internal stability testing

We test to ensure your products remain stable for its entire shelf life.

Stability testing programs are required to demonstrate that a product or raw material can meet or exceed its stated shelf life under different environmental conditions, such as temperature and humidity.

We have a range of comprehensive product stability testing services across internationally recommended storage profiles. After manufacturing of your product, we can conduct shelf life studies to suit your market.



Our expert knowledge and historical experience of material stability performance are then integrated into our product formula development process to ensure minimal formulation changes are required across the product’s life cycle.  

Our stability testing conditions:
Refrigerated: 5°C
Zone II (Mediterranean/subtropical): 25°C/60% RH
Zone IVa (Hot humid/tropical)​: 30°C/65% RH
Zone IVb (Hot/higher humidity): 30°C/75% RH
Accelerated: 40°C/75% RH

Our in-house Chemical and Microbiological Laboratories

We have unique capabilities with our own internal, custom built TGA compliant Chemical and Microbial testing laboratories on site at our production facility. These are equipped with the latest testing equipment to ensure compliance with strict quality standards. On site laboratory testing delivers benefits of greater consistency, reliability and efficiency, as well as the ability to respond and quickly react to any technical challenges. In addition, having our own in-house facility, reduces potential delays and inflexible timings, often associated with reliance on external laboratories.

Our extensive in-house testing capabilities include;
Total Aerobic Microbial Count
Total Yeast and Mould Count
Bile-tolerant Gram negative bacteria
E.coli Detection
Staphylococcus Detection
Salmonella Detection

Our industry leading Probiotic Testing Capabilities

We are Australia’s first fully compliant TGA probiotic manufacturing facility, with in-house capability to apply the latest TGA probiotic testing compliance requirements;

Species-level identification using validated analytical methods (qPCR for DNA sequencing, identification and quantification)
Viability and enumeration testing
Stability studies
Water activity testing

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