Curia lays out plans to expand complex API manufacturing capacity

The $35 million investment will more than double the site’s batch-size scaling and product output.
Curia has announced it plans to invest more than $35 million in expanding its commercial API manufacturing capacity at its Rensselaer, New York facility.
The CDMO, which was formerly known as AMRI, has said the increased production capacity and product-handling solutions will strengthen its ability to manufacture small-scale to large-volume complex APIs for its current and future partners.
The $35 million investment will include new vessel capacities that more than double the site’s batch-size scaling and product output. It will also allow for the introduction of a variety of new products and enable Curia to meet growing demand for high potency API manufacturing.
Curia Chairman and CEO John Ratliff said: "The engineering and technology advances we have designed for the site will enhance our flexibility, efficiency and scale, allowing us to meet our customers’ current and future complex manufacturing needs.”
Integral to the expansion are plans to optimise energy usage and enhance environmental standards.
Curia’s Rensselaer facility currently produces APIs to meet the development and commercial needs of more than 50 products, including critical oncology therapeutics and novel treatments addressing unmet medical needs.
Last year, it was the first facility in the industry to be designated 'Industry Leader' as part of its re-certification under the independent SafeBridge program for “Potent Compound Safety Certification”.
The expansion is expected to be completed within 18 months and generate new technical jobs in Rensselaer.

Related News
-
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 Pharma Supply Chain People Moves
The latest appointments, promotions, and structural changes across the pharmaceutical supply chain. -
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. -
News BIOSECURE Act continues to loom over Chinese pharma manufacturers
With the US BIOSECURE Act on its way to passing into legislation, Chinese companies are facing declining revenues within the first half of 2024 as US pharmaceutical and healthcare companies pull their businesses from the country. -
News Ophthalmologic drug product Eylea faces biosimilar threats after FDA approvals
Regeneron Pharmaceutical’s blockbuster ophthalmology drug Eylea is facing biosimilar competition as the US FDA approves Biocon’s Yesafili and Samsung Bioepis/Biogen’s Opuviz.
Recently Visited
Position your company at the heart of the global Pharma industry with a CPHI Online membership
-
Your products and solutions visible to thousands of visitors within the largest Pharma marketplace
-
Generate high-quality, engaged leads for your business, all year round
-
Promote your business as the industry’s thought-leader by hosting your reports, brochures and videos within your profile
-
Your company’s profile boosted at all participating CPHI events
-
An easy-to-use platform with a detailed dashboard showing your leads and performance