CDMO Services for Complex Dosage Forms
We offer end-to-end CDMO development for nasal sprays, semi-solids and pre-filled syringes. Whether you’re developing generics, innovative concepts, OTC or prescription medicines, we support your full development pathway. With all essential expertise available in-house, we support the preparation of regulatory dossiers and manage submissions, while also providing commercial-scale manufacturing to ensure a seamless transition from development to market supply.
What We Deliver
- Complete pharmaceutical development from idea to commercialisation
- Formulation expertise in nasal, topical and injectable dosage forms
- Advanced analytical method development and validation
- Manufacturing of registration batches, including testing and stability programs
Why choose Basic Pharma for nasal spray CDMO services?
We offer a full suite of end-to-end CDMO capabilities for nasal spray drug products.
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Formulation and packaging development
Our team develops both new and generic formulations, from nasal sprays, creams, ointments and gels to sterile pre filled syringes. We offer troubleshooting, process optimization and scale-up support. Packaging development covers all related delivery formats—such as spray systems and pre-filled devices.
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Analytical Development
We provide analytical method development and validation (HPLC), along with development testing such as rheology, cascade impaction, droplet size distribution and spray pattern. Furthermore, our capabilities include full stability studies to support development, registration and shelf-life determination.
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Risk analysis
We conduct comprehensive risk assessments covering extractables and leachables, elemental impurities, nitrosamines and excipient-related risks, supporting safe and compliant product development.