Phase I, II and III Clinical Supply

Upperton Pharma Solutions

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Upperton provide clinical supply for Phase I, Phase II and Phase III, specialising in oral, nasal and pulmonary dosage forms. Our services include:

Phase I-II Clinical Supply

Clinical Manufacturing: Production of clinical trial materials for Phases I and II
QC Testing: Quality control testing to meet regulatory standards
ICH Stability: Stability testing following (ICH) guidelines
Qualified Person Release: Ensuring product release complies with regulatory requirements
Clinical Stability: Assessing the stability of clinical trial materials throughout development

Process Scale-Up for Phase III

Method Validation: Validating analytical and manufacturing methods for Phase III trials
Cleaning Validation: Verifying cleaning processes to maintain product quality
ICH Stability: Stability testing to support Phase III trials and registration.
QP Release: Ensuring final product release meets all regulatory and quality standards

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Phase I, II and III Clinical Supply