Support for your semi-solid project needs
Recipharm can support all your semi-solid development and manufacturing project needs.
As a global CDMO, we have a wealth of experience tackling the challenges associated with the development of semi-solids, from managing chemical stability, to physical stability and dose homogeneity.
Your partner for semi-solid formulations
We produce a wide range of both topical and transdermal semi-solid dosage forms, including:
- Creams
- Gels
- Ointments
- Pastes
- Suppositories
End-to-end development support for semi-solid products
We can support at all stages of the development process, performing characterisation work, including chemical analysis as well as rheology, to deliver the perfect product for your needs.
General drug substances, as well as controlled drugs, are handled within Recipharm's semi-solid dose manufacturing facilities.
FACT SHEET | GENERIC SEMI-SOLIDS – AN OVERVIEW OF CURRENT REGULATORY REQUIREMENT
RELATED | Dowload Recipharm's Full Service Offering Fact Sheet
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Partner with Recipharm for your semi-solid dose projects
Looking for a CDMO partner to help with topical and transdermal semi-solid project needs? Recipharm's global presence and expertise can help your project accelerate from development through to commercial manufacturing. Contact us to discover how.
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