Recipharm
Contract development and manufacturing organization offering development and commercial manufacturing services for topical and transdermal semi-solid drug products. Services cover formulation, analytical characterisation (including rheology), stability and dose-homogeneity assessment, technology transfer, packaging and regulatory support. Facilities handle both general and controlled drug substances for semi-solid dosage forms.
Industries
Nr. of Employees
Very Large (1000+)
Services
Formulation development and commercial manufacturing for topical and transdermal semi-solid dosage forms.
Analytical development and testing including chemical analysis and rheology to support formulation, stability and release testing.
Transfer of data, materials and knowledge between development and manufacturing sites to enable scale-up and commercial manufacturing.
Packaging solutions for semi-solid products to meet product and regulatory requirements.
Regulatory guidance for semi-solid products and controlled substances, including navigation of applicable requirements.
Formulation development and commercial manufacturing for topical and transdermal semi-solid dosage forms.
Analytical development and testing including chemical analysis and rheology to support formulation, stability and release testing.
Transfer of data, materials and knowledge between development and manufacturing sites to enable scale-up and commercial manufacturing.
Packaging solutions for semi-solid products to meet product and regulatory requirements.
Regulatory guidance for semi-solid products and controlled substances, including navigation of applicable requirements.
Expertise Areas
- Semi-solid formulation development
- Topical and transdermal drug-product manufacturing
- Analytical development and rheological characterisation
- Stability testing and dose uniformity
Key Technologies
- Rheological analysis
- Chemical stability testing
- Dose uniformity testing
- Semi-solid formulation techniques