CDMO services for medicated chewing gum and cannabinoids

CDMO SERVICES

Pharmaceutical development and formulation services

We offer pharmaceutical development and formulation services for chewable oral dosage forms, aimed at converting complex APIs into controlled and reproducible dose units. The approach integrates process robustness criteria and readiness for industrial scale-up, supported by expertise in advanced formulation and manufacturing-oriented design.

Manufacturing for clinical trials and clinical supply

We support the transition from development to the manufacturing of batches for clinical trials and the supply of product in regulated environments, with a focus on batch-to-batch consistency, traceability and readiness for scale-up. The approach is applicable to therapeutic cannabinoids and other botanical-derived APIs, enabling their integration into a standardized pharmaceutical dosage form intended for clinical programs across different indications.

Regulatory support and documentation for pharmaceutical partners

We integrate regulatory support and technical documentation as part of the CDMO service, facilitating pharmaceutical companies and industrial partners in advancing their clinical development programs. The approach combines regulatory expertise with an industrial perspective, enabling early decisions oriented toward manufacturing feasibility, regulatory compliance and long-term pharmaceutical development.
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Professional contact

Medical Flowers Developments collaborates with pharmaceutical and biotech companies interested in cannabinoid clinical trials. The company maintains an open approach to professional discussions focused on development, innovation, and investment in regulated projects.