A Comprehensive GMP service

Following from our work in physical form screening (polymorphism, salt selction etc), physical property testing (comprehensive preformulation) and formulatyion development, Pharmaterials can transfer to our in house cGMP facility in Hunt Valley USA.  The transfer will be managed by the Pharmaterials formulation staff giving a seemless transition.

The 230,000 sq ft cGMP facility comprises 36 production rooms, 14 containment suites and 1 low humidity suite.

Services include:

• Clinical trial manufacture for phase I, II, III and IV
• Commercial manufacture
• high potency / cytotoxics
• sterile products
• tablets/capsules – all types
• soft gelatine capsules
• liquid filled hard gelatine capsules
• ICH Stability testing
• Analytical services

 For further details see www.pharm-int.com