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Drug products

Nuvisan provides comprehensive drug product development services, delivering end-to-end solutions from formulation design to clinical trial supplies. Specialising in non-sterile oral and topical dosage forms, we offer advanced preformulation studies, formulation screening, stability assessments and in vitro testing. We are committed to applying novel approaches and established techniques to create tailored solutions for diverse compounds, indications and clients, with a strong focus on quality.

Our team has a proven track record of developing effective formulas that have supported several commercially successful topical products. These achievements reflect our strong emphasis on innovation and a focus on the needs of patients and healthcare professionals. Nuvisan's formulation development services, including consulting, help accelerate time to proof-of-concept, providing a solid foundation for clinical development and commercialisation.
Formulation scientist preparing a light pink solution using a typical lab-scale mixer

Preformulation

Our state-of-the-art laboratories are fully equipped for efficient preformulation and development of solutions, gels, creams and capsules. Nuvisan's highly experienced scientists develop varied formulation concepts that de-risk formulation development while ensuring efficiency, effectiveness and robustness. In parallel, our compositions provide appropriate delivery, stability, tolerance and sensory characteristics.

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Two hands in gloves doing cream formulation

Formulation development of non-sterile dosage forms

Nuvisan specialises in non-sterile dosage form development, including tailored topical, semi-solid and liquid formulations. We select excipients to meet molecule and indication needs to support the creation of effective, well-tolerated and elegant formulas that enable successful scale-up. Our robust formulation process, grounded in experience with marketed products, is designed to manage risks and maximise clinical study potential.

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A scientist is pouring powder into a manufacturing vessel

GMP manufacturing of non-sterile dosage forms

Nuvisan provides GMP-compliant manufacturing services for non-sterile dosage forms, including topical, semi-solid and liquid formulations. Our state-of-the-art facilities ensure the highest standards of quality and regulatory compliance, supporting the production of scalable, safe and effective products.

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Blue door showing through a glass lab coats

In vitro tests

Nuvisan offers comprehensive in vitro testing services to support drug development, including permeation studies, in vitro release testing (IVRT), in vitro pharmacodynamic tests (e.g., inflammation platform) and in vitro toxicity tests. Using advanced techniques like in vitro skin permeability testing (IVPT) with human skin explants, we provide critical data on drug delivery to enable formulation optimisation. This data, combined with in vitro toxicity tests, supports safety assessments. Our in vitro testing facilitates the effective and targeted development of dermatological products.

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