Semi Solid Formulation Development & Manufacturing

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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 requirements

FACT SHEET | Recipharm's full service offering

Related services

Our integrated network of experts ensures trusted speed across every stage, from formulation to packaging.

Analytical services comprehensive support for a range of analytical development services
Pharmaceutical packaging a range of packaging solutions to meet your product needs
Technology transfer support in seamless transition of data, materials and knowledge
Regulatory delivering regulatory excellence for customers across the globe

Recipharm, your CDMO partner

Looking for a partner for your 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

Related resource

Navigating the regulatory landscape for controlled substances

Drug substance