What is CMC in Pharmaceutical Development?
CMC refers to the set of activities that ensure a drug product is consistently produced, controlled, and meets the required quality standards.
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CMC in the Drug Development Process
Without a strong CMC strategy, even a promising drug candidate can fail to reach the market. Discover the foundation for product development.
Navigating CMC Regulatory Requirements in the Drug Development Process
The CMC section of a regulatory submission is essential as it ensures that the final product can be manufactured consistently and reliably.
Upperton Pharma Solutions Named Winner in 2025 CDMO Leadership Awards
Upperton is proud to announce its selection as a winner in the Small Molecule Dosage Form category at the CDMO Leadership Awards.
Ensuring Successful Technology Transfer: The Role of Quality Management Systems
A well-implemented Quality Management System (QMS) is the backbone of a successful technology transfer. Learn more in our guide.
Navigating Technology Transfer in Pharmaceutical Manufacturing: Best Practices
Tech transfer is the process of moving a product’s manufacturing process, related knowledge and documentation, from one facility to another.
Management Spotlight with Danielle Young
Discover more about our team. In this Spotlight, meet our QC Manager, Danielle Young, on her journey with Upperton.
What It Means for Upperton to Be a Living Wage Employer
We’re delighted to share that Upperton has officially been accredited as a Living Wage Employer, joining over 15,000 UK employers.
Upperton Celebrates International Day of Women and Girls in Science
To celebrate International Day of Women and Girls in Science, we raised funds for Plan International, a charity dedicated to gender equality.
Upperton Completes Build of New £7m Sterile Manufacturing Facility
Upperton completes build of new £7m Nottingham sterile manufacturing facility for parenteral, nasal and pulmonary delivery.
