Juniper and Crystec sign agreement for next-generation medicines
Juniper Pharma Services, a subsidiary of Juniper Pharmaceuticals, will work with CrystecPharma on a major multi-partner project as part of the Advanced Manufacturing Supply Chain Initiative (AMSCI) to help create a new platform to accelerate drug development in the future.
Both companies will collaborate as part of this UK-based consortium of partners that includes two of the world’s biggest pharmaceutical companies. The programme aims to develop and demonstrate the capability of supercritical fluid technology in manufacturing smarter, higher quality pharmaceutical products, whilst moving products more quickly from research to the marketplace.
In just 3 years, AMSCI is expecting the joint platform to create products from concept to manufacture.
CrystecPharma designs crystals and particles aimed at meeting targeted performance requirements of a medicine. Juniper Pharma Services will bring its expertise in characterisation, formulation development and GMP production to the supercritical fluid manufacturing platform.
Dr Nikin Patel, president at Juniper Pharma Services, said: “Working with CrystecPharma in collaboration with the other AMSCI partners is very exciting, as this alliance will produce a real step change in the advanced manufacturing of next-generation medicines.”
As a result of the project, CrystecPharma will refocus its manufacturing capability from China to the UK, working with Juniper Pharma Services as its international contract development and manufacturing organisation (CDMO) partner. The technology company aims to develop three new products through this programme.
Paul Thorning, CEO at CrystecPharma, said: “Such a collaborative campaign has the potential to really demonstrate the global competitiveness of the UK in pharmaceutical technology development and manufacturing.
“It will benefit from the invaluable expertise of the team at Juniper, which will enable our novel technology to move into a GMP compliant environment. Working closely with Juniper in this way allows us to rapidly establish the manufacturing capabilities needed to see us through to clinical trials.”
With an established track record of helping pharmaceutical companies and emerging biotechs to creatively develop new products and platforms, Juniper Pharma Services is able to mitigate risk and optimise formulation performance through its science-led approach to projects.
This is the latest major project for the CDMO after it entered into a long-term collaboration with OxSonics to support the development, scale-up, and GMP manufacturing of OxSonics’ proprietary sono-sensitive particles.
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.