Microneedle Medical Device CDMO

Project-specific development, registration support and manufacturing services for microneedle medical-device programs.

Technology / Product Concept

Microneedle arrays can be designed with product-specific structure and use conditions to create temporary micron-scale pathways in the stratum corneum. Dimensions and performance require product-specific verification.

Intended Use & Regulatory Considerations

Intended use, mechanism of action, classification and target market should be clarified before detailed development. CASMN can support early classification and registration-strategy assessment.

Development Workflow

Concept definition → prototype development → performance evaluation → process development → validation and registration support → manufacturing planning.

Validation & Manufacturing Support

Scope may include prototype preparation, selected performance evaluation, process validation support and scale-manufacturing planning for the agreed product pathway.

Potential Application Directions

Potential pathways include dermatology, aesthetic aftercare, localized care, pain management and drug-device combinations. Suitability depends on the defined product and intended use.

Cooperation Models

Programs can be structured around a client-held marketing authorization, commissioned R&D, contract manufacturing, or customized supply under an applicable CASMN-held authorization.

Request a Medical Device Development Plan

Send your target product, payload, development stage and cooperation scope to our business development team.

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