Contract research & development

We combine scientific expertise, specialist regulatory knowledge and practical manufacturing insight to develop effective, compliant products that meet the exacting requirements of your intended markets.

Whether you’re starting with a brand-new idea or refining an existing formulation, we provide end-to-end R&D support, from concept, formulation, and packaging design through to regulatory approval and market launch.

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Our team works across prescription and over-the-counter medicines, dietary supplements, nutraceuticals, and personal care products, as well as selected medical devices, for both human and animal health markets.

The Jaychem advantage

Multi-market expertise

Our team has successfully registered over 100 human and animal medicines in markets including NZ, AU, EU, US, Canada, and more.

Integrated capabilities

With in-house laboratories, regulatory affairs specialists, and manufacturing facilities, we streamline your path to market and protect your IP.

Proven track record

From small-batch trial products to large-scale commercial launches, we have the experience, infrastructure, and flexibility to make it happen.

Collaborative approach

We work closely with you to balance performance, compliance, and cost, ensuring your product is right for its intended market and consumers.

End-to-end product development expertise

Our research and development service covers the full journey from concept to market-ready product.

Creating new products or modifying existing ones to meet market, client, or regulatory needs, including generics and combination products.
Determining the optimal delivery form (liquids and semi-solids) and packaging for stability, compliance, and consumer appeal.
Evaluating your product’s requirements in each target market, identifying formulation or labelling changes to ensure compliance.
Designing and validating analytical methods to support product quality and regulatory submissions.
Conducting real-time and accelerated stability testing to international climatic zone requirements.
Manufacturing trial batches, coordinating third-party clinical testing, and providing support for blinded clinical trials to enhance objectivity and integrity.
Improving formulations, processes, and packaging for cost efficiency, quality, and market performance.