A Comprehensive cGMP service
FIRST IN MAN FAST
We are committed to rapid development of your compound. In keeping with your needs we will perform salt selection, polymorphism, preformulation, assay development, preclinical formulation and phase 1 formulation development. The product can then be manufactured in our new facility in Reading. The same team will take you through this process, with no need to transfer information and the ability to streamline the process to meet the most demanding timelines possible
The PII facility will be used for larger scale projects, up to commercial, and comprises 230,000 sq ft of cGMP with 36 production rooms, 14 containment suites and 1 low humidity suite.
Pharmaterials / PII services include:
- clinical trial manufacture for phase I, II, III and IV
- commercial manufacture
- high potency / cytotoxics
- sterile products
- tablets/capsules – all types
- soft gelatin capsules
- liquid filled hard gelatin capsules
- ICH Stability testing
- analytical services
For further details please contact us.
For further details on PII see www.pharm-int.com