Hours: 8:30 AM–5:30 PMSales: +86 10 8928 7035Business: bd@casmn.com

A development platform from delivery-route innovation to scale-up

Microneedle Drug Formulation CRO/CDMO

End-to-end development support for microneedle drug products, from feasibility and formulation to pilot scale-up, clinical batches and commercialization.
01

What Is Microneedle Drug Delivery?

Microneedles create micron-scale pathways through the stratum corneum to enable transdermal or intradermal delivery while avoiding the pain and usability limitations associated with conventional injections.

02

Suitable Modalities and Applications

The platform can evaluate innovative and improved drug products across multiple therapeutic areas and payload classes.

  • Metabolic medicines, including GLP-1-related programs
  • Local anesthetics and pain-management products
  • Neurology and sleep-related small molecules
  • Dermatology and local anti-inflammatory products
  • Peptides, proteins and nucleic-acid payloads
  • Intradermal vaccine delivery
03

CRO/CDMO Development Workflow

Feasibility assessment → formulation development → process development → preclinical support → pilot scale-up → clinical-batch preparation → IND-support documentation → commercial manufacturing support.

04

Evaluation and Quality Capabilities

Available methods include microneedle morphology, insertion and mechanical testing, HPLC analysis, stability studies, and release or permeation evaluation using IVRT/IVPT approaches.

Microscopic morphology of microneedle tipsMicroneedle mechanical force-displacement testCASMN HPLC analytical laboratory
05

How to Start a Project

A project normally begins with the active ingredient, target dose, intended application, development stage and expected regulatory pathway. CASMN then proposes a feasibility and development plan.

Discuss a Microneedle Drug Project

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

Email bd@casmn.com