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Oral Liquid Manufacturing

Efficient clinical and commercial-scale oral liquid manufacturing with the compliance infrastructure, quality controls, and manufacturing expertise your program demands.

Our Oral Liquid Capabilities

Flexible, scalable manufacturing built for clinical and commercial demands.

Licensed Controlled Substance Manufacturing

Active manufacturing licences for controlled substance oral liquids are in place, operational, and embedded in daily practice. The licence, the vault infrastructure, and the chain of custody systems are already built.
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Commercial-Scale
Oral Liquids

Syrups, solutions, and suspensions across paediatric, geriatric, oncology supportive care, and specialty pharma programs. Controlled and non-controlled formulations supported within one GMP facility.
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Integrated QC and Analytical Support

In-process controls, visual inspection, and finished product QC testing performed within the same facility as manufacture. Every batch released to exacting GMP standards with full chain of custody documentation for controlled substance programs.
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cGMP from Start to Finish

From formulation development through to GMP batch release, every program is managed within one accountable team and one GMP environment.
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    Formulation to Distribution in One Place

    BioCina expert setting up bioprocess development equipment to optimize clinical batch production for partners.

    Formulation Development

    Your formulation is assessed and optimized for stability, solubility, and regulatory requirements. Analytical methods are developed and validated before manufacture begins.
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    Raw Material Receipt

    All incoming materials are sampled, QC released and handled under controlled substance protocols where applicable.
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    Compounding
    and Filling

    Bulk liquid is prepared under GMP-controlled conditions and filled via the Farmomac line, with fill volume verification and in-process controls at every stage.
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    Closure and Labelling

    Tamper-evident, child-resistant closures can be applied and primary labelling completed within the same GMP environment.
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    Inspection, QC, and Batch Release

    Every unit is visually inspected before secondary packaging. Finished product QC testing and GMP batch release are completed with full chain of custody documentation for controlled substance programs.

    Product Categories We Support

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    Controlled Substance Oral Liquids

    More than 30 years of licensed controlled substance manufacturing experience. Active Schedule 8 licences, vault storage, diversion controls, and chain of custody protocols embedded as standard practice, with established export to New Zealand.
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    Pediatric Formulations

    Syrups and oral solutions for patients unable to swallow tablets, with the dosing accuracy and palatability paediatric programs require.
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    Geriatric Oral Liquids

    Liquid medicines for geriatric patients, formulated for ease of administration and patient compliance.
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    Specialty and Generic Oral Liquids

    Commercial-scale manufacturing for specialty pharma and generic oral liquid programs pursuing TGA, FDA, EMA or equivalent registrations.

    Did you know manufacturing in Australia could fund nearly half your program?

    Learn More
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    Drug Product Manufacturing Track Record

    0+ years
    of Sterile Manufacturing Heritage
    0M+ units
    Annual Capacity
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    0+
    Approved Products
    0+
    Countries Delivered
    Automated filling line for oral liquid pharmaceutical products, showing bottles being filled with precision.

    Ready to Start Your Oral Liquid Program?

    Our team is ready to discuss your formulation, licensing requirements, and path to commercial supply.