- What we do
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Routes of delivery
- Oral
- Nasal
- Pulmonary
- Parenteral
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Development stage
- Pre-clinical
- Phase I to Phase II
- Phase III - Commercial
Our Approach
- Project Management
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- About us
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A CDMO like no other
- About Us
- Our Facilities
- Our History
- Awards and Achievements
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Leadership Expertise
- Executive Leadership Team
- Board of Directors
- Careers
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- Resources
- Contact
Quality Control
and Assurance.
Explore Upperton's state-of-the-art QC labs
Expertise
Our Leadership team has extensive collective experience in steering products from pre-clinical to commercial manufacture.
Science-led
Our approach is scientific, collaborative and open, ensuring an open dialogue and transparency that fits your project.
Award-winning
We are a leading CDMO recognised for numerous awards including a King's Award For Enterprise.
Nimble
We adapt to your project needs, and pledge to never relegating it to the bottom of the list.
Our comprehensive Quality Control services encompass the full spectrum of method development, transfer, qualification, and validation, supported by a state-of-the-art Quality Control and Analytical laboratories.
Collaborative and science-led
Our approach.
We offer comprehensive Quality Control services to ensure the highest standards of compliance and product safety in pharmaceutical development and manufacturing.
Commitment to Quality and Regulatory Excellence
Our Quality Control and Analytical Laboratory.
Our dedicated 8,000 sq ft Quality Control and Analytical laboratories feature dedicated HPLC and dissolution laboratories alongside small molecule and biological test equipment. With humidity-controlled areas for moisture-sensitive products, our facilities are designed to support our clients from the earliest stages of product development to GMP manufacturing, ensuring that every step meets the most stringent quality standards.
Our Quality Control Services
Raw Materials Testing: Ensuring all starting materials meet required quality specifications
Finished Product Release Testing: Comprehensive testing for final product release.
In-Process Testing: Monitoring during production to ensure consistent quality.
Cleaning Verification: Verifying the cleanliness of manufacturing equipment post-production.
Stability Testing (ICH): Assessing product stability under a variety of conditions in line with ICH guidelines.
Environmental Monitoring: Ensuring clean and controlled environments for manufacturing.
Full Method Validation: Developing and validating methods to ensure accuracy and reliability in testing.