Eckert & Ziegler expands CDMO services to support radiopharma companies
Having acquired a 53,000 sq-ft property in Berlin, the company plans to set up new laboratories, production and cleanrooms
Eckert & Ziegler Strahlen- und Medizintechnik has acquired a site in Berlin from which it can expand its contract development and manufacturing services for a variety of cancer therapeutics and radio diagnostics among others.
The Berlin City Government has granted the company a 66-year lease for the industrial property, which includes 53,000 sq. ft (5,000 m2) of factory floor, located at the north eastern limit of the city.
The group said it plans to expand its services to accommodate a variety of cancer therapeutics and radio diagnostics to support companies developing new radiopharmaceuticals.
Dr Lutz Helmke, COO of Eckert & Ziegler's medical division suggested the company may, at a later date, use the site to manufacture proprietary drugs and diagnostics.
The renovation, which will include installing new laboratories, GMP production and cleanrooms, and the creation of high-tech workplaces, will cost up to €10-mm. Both the acquisition and the renovation is part of the CDMO's €100-mm global capacity expansion programme.
Production processes developed and validated in Berlin will be duplicated in the company's US and China sites so that customers can receive identical and standardised components for their radiopharmaceuticals.
The new site is expected to meet the highest energy efficiencies given its proximity to a thermal power station.
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.