Product development & technology transfer

Our technology transfer service ensures that novel to generic products are transitioned into Jaychem’s facility smoothly, with no compromise on quality, compliance, or timelines.

Every transfer starts with a deep technical review — understanding the formulation, processes, packaging, and market requirements — before adapting and validating them for our plant. This ensures the product performs exactly as intended, meets all regulatory standards, and can be scaled reliably for its target markets.

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We regularly take over production from facilities that can’t meet the regulatory requirements of new markets, scaling processes to our GMP-certified environment and integrating them with our quality and testing systems to maintain continuity of supply.

A transfer can also be the ideal moment to refine a product, adjusting a formulation, improving shelf life, or updating packaging for new markets. Our development team works alongside the transfer process so improvements can be implemented without delaying launch.

The Jaychem advantage

Market expertise

Our team has handled transfers for products going into highly regulated markets such as Australia, the EU, Canada, and the US — ensuring they meet Medsafe, TGA, ACVM, APVMA, and FDA requirements.

Thorough pre-transfer assessment

We review everything from raw materials and suppliers to equipment set-up, batch records, testing methods, packaging, and stability data before the first trial run.

Adaptable scale-up

We can match your current volumes or increase output to meet growth targets, running small validation batches or moving directly into large-scale production.

Integration with quality systems

Transferred processes are embedded into our GMP framework, backed by robust documentation, validated cleaning procedures, and full traceability.

Our technology transfer process

A systematic approach combining technical rigour, regulatory precision, and operational efficiency.

Assessment of the product’s formulation, process, analytical methods, packaging, and market requirements, identifying any changes for compliance or efficiency.
Translating your manufacturing and testing procedures into our facility, refining them if needed for GMP or market-specific regulations.
Verifying that our equipment, or newly installed machinery, meets your product’s requirements and maintains quality consistency.
Replicating or modifying packaging to meet regulatory, market, or language requirements, from label claims to tamper-evident seals.
Executing process validation batches to confirm the product performs consistently to specification.
Preparing and supplying technical documentation for regulatory submissions related to the transfer.