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The facility gives the green light to support clients from formulation development to late-phase clinical manufacture and product registration.
July 18, 2024
By: Tim Wright
Editor-in-Chief, Contract Pharma
Upperton Pharma Solutions, a contract development and manufacturing organization (CDMO), has completed a Medicines and Healthcare products Regulatory Agency (MHRA) inspection at its newly commissioned 50,000 square foot development and GMP manufacturing facility in Nottingham, UK.
This milestone inspection, conducted by the UK Government’s regulatory authority, marks a significant achievement for Upperton Pharma Solutions following the completion of the build, commissioning, validation and approval of the facility in just 18 months. With the successful MHRA inspection approval, Upperton Pharma Solutions has enhanced its offering, supporting the development of oral, nasal, and pulmonary drug products underpinned by the capability to provide Phase I, II, and III clinical supplies.
“We are absolutely delighted to achieve this milestone,” said Nikki Whitfield, CEO of Upperton Pharma Solutions. “We have been conducting manufacturing scale-up activities since the start of the year following the installation of the larger scale solid oral dosage form process trains and this gives the green light for our GMP facility to support clients right through to late-phase clinical manufacture and product registration.”
The successful MHRA inspection enables Upperton Pharma Solutions to seamlessly transition from research and development (R&D) to GMP manufacturing and commercialization on one site, following recent investment in large-scale process equipment including a Gerteis Mini-Pactor , GEA Post Hoist Blender, O’Hara M50 Tablet Coating System and a ZANASI 40 Capsule Filler.
Capable of handling batch sizes of up to 250kg and a wide variety of dosage forms, such as solids, liquids, semi-solids, nasal and inhaled pharmaceuticals, including potent molecules and controlled drugs, the MHRA approval signals Upperton’s transition into an integrated CDMO.
Paul Kelsall, director of clinical manufacturing, Upperton Pharma Solutions, said, “This is a dedication to the tremendous hard work our colleagues have put in to achieve the targets and aspirations of our business. We are looking forward to working with our clients and offering services from early-stage development through to late-stage clinical manufacture and product registration. These are exciting times for Upperton as we continue to move forward and expand our capabilities.”
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