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