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Pharmaceutical Development

Solid dosage form, injectables and freeze-dried forms

Our teams of specialists offer support and guidance in the development and large-scale production of your products. We take your molecule end-to-end until the drug product to allow your clinical trials and product filing.

flexible and highly effective production facilities

 
We bring all our expertise to bear on achieving your projects:
 
  • Feasibility study
  • Pre-formulation & formulation, characterization, galenical development
  • Process development and validation
  • Process optimisation
  • Analytical method development and validation services
  • ICH stability studies
  • Documentary and regulatory support

Lundbeck CDM with you, from the pre-clinical to regulatory approval phase

We offer high flexibility, technical expertise and experience to develop and produce your oral solid and sterile drug products.

Research Tax Credit agreement (CIR)

Your development projects are eligible for the Research Tax Credit (CIR) up to 30% of the amount. 

We have obtained the Research Tax Credit agreement from the French Ministry of Higher Education, Research and Innovation (MESRI) to execute R&D activities for third parties. 

  • Download Elaiapharm Research Tax Credit (CIR) accreditation

    • More from Lundbeck CDM SERVICES

    Solid Dosage

    Our production systems meet current safety, environmental and quality standards, with recognized procedural knowledge in the development and manufacturing of tablets and micro-tablets.

    Sterile Forms

    We manage the development and manufacturing of injectables freeze-dried and liquid products in vials.

    Packaging

    We manage primary and secondary packaging services in blisters, bottles
    and kits.