Upperton Announces Sterile Drug Manufacturing Investment

Upperton Pharma Solutions announced a significant expansion into sterile drug manufacturing with the launch of a new c. $6.3 million GMP facility. The company said that the state-of-the-art facility is designed to meet the growing demand for sterile product development and manufacturing services - particularly for biologics and small molecule drugs - and that it will enhance their capabilities in formulation development, clinical trial manufacturing, and commercial drug product supply.

Leading UK contract development and manufacturing organisation (CDMO) Upperton Pharma Solutions (Upperton) has announced a £5million investment to expand operations into small-scale sterile fill-finish.

After completing the build and qualification of a new 50,000sqft GMP facility during 2023, the UK-based CDMO announces further expansion at its Trent Gateway site to include sterile capabilities with a purpose-built facility designed specifically in line with the revised EU GMP Annex-1 regulations.

The £5million investment into an additional 7,000sqft sterile manufacturing facility at Trent Gateway, follows a period of significant growth in demand for the formulation development and manufacture of sterile and terminally sterilised products.

Nikki Whitfield, CEO of Upperton Pharma Solutions, said, “This investment addresses a real shortage within our industry of providers of small batches of sterile drug products to support early clinical trials. Given our existing formulation development and analytical capabilities, it represents a natural progression for Upperton and an exciting milestone in our growth plans.”

The sterile facility, designed in line with the EU GMP Annex-1 Revisions, will use advanced VHP isolation technology and carry out GMP fill-finish of sterile drug products for biologics and small molecules, making use of existing full-service formulation development and quality control labs. The facility will support the manufacturing of aseptic and terminally sterilized small volume liquids for parenteral, ocular and pulmonary delivery.

The facility build is scheduled to begin in February 2024 with the facility commissioning and validation to be completed in early Q4 / 2024.

This investment in sterile drug product manufacturing enhances the existing service offering, which provides formulation development across a broad range of dosage forms, clinical trial supply, and niche-scale commercial manufacture for non-sterile dosage forms.

Nikki adds, “Our leadership team fully understand the challenges of getting our clients from pre-clinical to early phase clinical studies quickly, whilst maintaining quality and regulatory compliance. The combined experience of our leadership team in sterile facility builds and subsequent operations ensures that we will enter this new market with confidence.”

For more, please find the original story source here.