Pharmaceutical Development
Solid dosage form
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
- 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 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.
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.
Packaging
We manage primary and secondary packaging services in blisters, bottles and kits.
Quality & HSE
Our Quality and HSE Management Systems guarantee our customers high standards of quality, safety and performance.