Sterling pilot plant facility expansion up and running
Additional three new reactor trains will help the CDMO to meet growing market demand for smaller API batch sizes.
CDMO Sterling Pharma Solutions has announced the expansion of its pilot plant facility is now operational at its UK site following a £6-million investment last year.
The new cGMP facility increases the existing pilot plant’s capacity by 33%, enhancing the CDMO’s scale-up capabilities and adding greater flexibility to cater for small to mid-scale clinical supply and commercial batch production.
The investment included the addition of three new reactor trains at scales of 225 L, 500 L and 1,360 L, which will help the company to meet growing market demand for smaller API batch sizes.
Kevin Cook, CEO at Sterling Pharma Solutions says: “We’ve experienced significant growth over the past few years and as demand rises, we have taken steps to bolster our offering.
“There are a number of increasingly complex products entering the drug pipeline, many of which are intended for smaller patient populations, so the ability to cater for smaller volumes will be essential as we move forward.
“In addition, increasingly our customers are coming to us for an end-to-end API development and manufacturing offering that will allow them to outsource the entire process. The expansion of our pilot plant will increase our scale-up abilities and allow us to cater for additional projects from proof-of-concept through to commercial manufacture.”
The investment will also allow Sterling Pharma Solutions to handle potent compounds across a range of equipment scales, complementing the company’s existing offering.
Related News
-
News Pharmaceutical Supply Chain People Moves
The latest appointments, promotions, and structural changes across the pharmaceutical supply chain.
-
News Merck KGaA to buy US biotech SpringWorks for US$3.9 billion
The German multinational pharmaceutical company Merck KGaA have signed a deal to buy US biotech company SpringWorks Therapeutics at an equity value of US$3.9 billion in a move to add rare cancer therapeutics to their pipelines.
-
News Cassava Sciences halts Alzheimer's drug trial after limited progress
Cassava Sciences have drawn a close to their investigations and development of the drug simufilam, which they intended to be used for the treatment of Alzheimer’s disease.
-
News US FDA adds haemodialysis bloodlines to devices shortage list
On March 14, 2025, the US FDA published an open letter to healthcare providers citing continuing supply disruptions of haemodialysis bloodlines, an essential component of dialysis machines.
-
News Vertex Pharmaceuticals stock jumps as FDA approves non-opioid painkiller
UK-based Vertex Pharmaceuticals saw their stock shares soar as the US FDA signed off on the non-opioid painkiller Journavx, also known as suzetrigine, for patients with moderate to severe acute pain, caused by surgery, accidents, or injuries.
-
News Lessons from CPHI Milan 2024: Sunny Intervals for Pharma Manufacturing?
As the 2024 CPHI conference wrapped up in Milan, we caught up with L.E.K. Consulting – a global strategy consulting firm with deep expertise in pharma manufacturing – to discuss evolving market perspectives and business outlook. -
News US BIOSECURE Act passed by US House of Representatives
The controversial act, which has already impacted several foreign companies operating in the US, was passed by the House of Representatives on September 9, 2024. It is now headed for the US Senate before it can be signed into law by President Joe Biden... -
News Drug prices agreed upon as part of the US Inflation Reduction Act
The Inflation Reduction Act brought into constitution by the Biden administation in 2022, which proposed a drug price negotiation between the government and pharmaceutical companies, has reached it's first agreement.