Laboratory Services

Backed by GMP certification, our laboratory applies rigorous testing and validation protocols to safeguard quality and ensure your product is both market-ready and regulatory-approved.

Fully integrated with our R&D, manufacturing, and regulatory teams, we deliver fast, reliable results for projects ranging from early-stage development to large-scale commercial production.

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From developing and validating new test methods to conducting stability studies across multiple climatic zones, our laboratory services support both novel and generic products in human and animal health, as well as dietary supplements, nutraceuticals, personal care formulations, and selected medical devices.

The Jaychem advantage

Integrated expertise

Our laboratory works alongside our R&D and manufacturing teams, streamlining the path from development to validation to market release.

In-house method development

We can design, develop, and validate new analytical and microbiological methods for products with unique specifications or regulatory needs.

Global regulatory alignment

We test to the requirements of Medsafe, TGA, FDA, EMA, and other authorities, supporting multi-market submissions and product launches.

Proven stability testing capability

Real-time and accelerated stability studies are conducted in controlled environments that simulate a full range of international climatic zones.

Laboratory services & capabilities

Specialist testing, analysis, and validation to support every stage of your product’s journey — from formulation to final release.

Comprehensive testing to confirm product quality, safety, and compliance with regulatory standards.
Designing, verifying, and transferring analytical methods to ensure accurate and reproducible results.
Detecting, analysing, and documenting impurities to meet quality and safety requirements.
Developing small-scale formulations and conducting stability testing for ICH climatic zones, in-use, routine, and special studies.
Assessing product stability and integrity during bulk storage prior to final packaging.
Evaluating the effectiveness of antimicrobial preservatives to ensure ongoing product safety.
Identifying and assessing elemental impurities in line with global regulatory guidelines.
Reviewing products against major pharmacopeial standards to ensure compliance.
Working with specialist laboratories internationally to test product performance and to justify label claims
Conducting GMP-certified QC, stability, and validation testing for both animal and human health products.