Dealing with all kinds of galenic development projects.
Risk management during industrial transpositions.
We understand and integrate transfer constraints on industrial sites and can adapt to all requirements.
In addition, our galenic experts deal with the various stages in a development project for galenic formulations involving one more active ingredients:
- Formulation, compatibility studies on active ingredients and excipients, choice of formulation and packaging,
- Development, scale-up, validation and industrial transfer of manufacturing processes,
- Optimisation of formulae and processes (possible scale-down),
- Completion of test batches,
- Supplying of pilot and clinical batches,
- Manufacturing of small ranges of commercial batches (from 1 to 150 kg).
Our galenic development sector works alongside a team of engineers with extensive experience in the field. It also possesses an in-depth understanding of transfer projects on production sites and is aware of the constraints of the industrial sector.
Thanks to regular investments, our service has access to modern equipment which corresponds to European and international statutory standards. It has access to a galenic laboratory for small-scale tests as well as a GMP production area for more extensive work and clinical and commercial manufacturing protects.
Galenic development – MULTI-FORM PHARMACEUTICAL PRODUCTS
Solid oral forms
- Immediate or controlled release tablets, coated or non-coated, orodispersible or dispersible, chewable or effervescent
- Soft capsules
- Powders, granules and microgranules in pouches and sticks
- Injectable liquids
- Haemostatic compresses
- Diagnostic reagents
- Creams, gels, ointments
- Nasal and eye drops
- Ophthalmic baths
- Eye solutions
- Nasal, auricular, topical and oral sprays