PMI BioPharma Solutions offer service "Clinical Trial Material Manufacturing"
Basic Information
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4.3(45)
Category
Subcategory & Sub-subcategory
Trade Type
Offer Service
Service Name
Clinical Trial Material Manufacturing
Service Provider(s)
Specifications
- Chamber Capacity: Onsite stability storage supporting Phase I and II trial material, with nearly all testing performed in-house
- Protocol Design: Analytical method development and validation integrated with in-house stability protocols
- Study Conditions: cGMP manufacturing and stability storage/testing for Phase I and II investigational products, covering liquids and creams via aseptic filling/finishing and microfluidization
Other Information
Additional Description:
PMI Bio delivers product development and cGMP manufacturing for Phase I and II trials, covering process development, non-sterile manufacture and filling of liquids and creams, aseptic filling and finishing, and microfluidization of liquids among other capabilities. Its team develops and validates analytical methods and offers onsite stability storage and testing, with nearly all testing performed in-house.
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