Solid Dosage Forms
Tablet and hard-capsule opportunities supported through technical evaluation, transfer, scale-up, manufacturing and packaging.
Explore solid dosage →INTEGRATED MANUFACTURING CAPABILITIES
Pharmaceutical Manufacturing
Dedicated dosage-form platforms supported by technical evaluation, technology transfer, scale-up, validation and commercial manufacturing pathways.
REF. JV-MFG-001MANUFACTURING APPROACH
Manufacturing platforms connected by one technical and quality framework.
Jean Vichar supports oral solid, pressurized inhalation and nasal delivery products through dedicated manufacturing platforms. Dry powder inhaler capability is available within the pharmaceutical ecosystem through Lirok Pharma.
Each opportunity begins with a technical assessment of the dosage form, formulation, process history, component requirements, documentation status and intended market. The outcome is a defined project pathway, not a generic production offer.
Product and platform fitReview formulation, process, components and intended commercial scope.
Technology transferTranslate existing knowledge and documentation into a controlled manufacturing pathway.
Scale-up and validationPlan progression toward repeatable commercial execution.
Packaging and lifecycle supportCoordinate packaging needs, technical changes and ongoing supply requirements.
REF. JV-PLAT-002PLATFORM PORTFOLIO
Four dosage-form pathways, with CMO/CDMO support across the lifecycle.
Metered Dose Inhalers
Pressurized inhalation products requiring coordinated formulation, component, filling, assembly and quality activities.
Explore MDI →Nasal Spray Systems
Metered nasal delivery products involving formulation, container-closure integration, filling, assembly and packaging.
Explore nasal sprays →Dry Powder Inhalers
DPI manufacturing capability within the ecosystem through Lirok Pharma, complementing Jean Vichar’s respiratory platforms.
Explore DPI →REF. JV-PROJECT-003PROJECT DEFINITION
What we review
- Dosage form and formulation status
- Process history and transfer package
- Analytical and quality documentation
- Device or packaging components
What we define
- Technical workstream and responsibilities
- Development, transfer or manufacturing scope
- Validation and documentation expectations
- Commercial and supply assumptions
What partners gain
- A coordinated technical pathway
- Earlier visibility of project risks
- Clear decision points and deliverables
- Continuity from evaluation to supply
Start with the product, not a predefined package
Tell us where your project stands and what the next commercial milestone needs to be.
Our team can assess platform fit, available documentation and the work required to move toward transfer, validation or commercial manufacturing.
Contact Jean Vichar