Merck Strengthens Commitment to Chinese Growth Market
Merck KGaA, has reiterated its commitment to investments in the Chinese market, strengthening a major pillar of its emerging markets growth strategy.
Merck’s Executive Board this week met in Shanghai, a month before the groundbreaking of its new pharmaceutical plant in Nantong, which from 2017 will be the group’s second-largest pharmaceutical manufacturing facility globally.
Merck currently employs more than 2,000 people at over 40 sites in China, with the most important products including Erbitux to treat cancer, Gonal-f to treat infertility, as well as life science tools and liquid crystals (LC) for flat panel displays. In total, Merck has committed more than €100 million to investments in China over the past 3 years.
“China is of strategic importance to Merck,” said Karl-Ludwig Kley, Chairman of the Executive Board. “Together with government officials, customers, partners and our highly motivated local colleagues, we will explore ways to further address critical healthcare needs of the Chinese population — both with our high-quality drugs and our life science tools for biopharmaceutical R&D. We’re also meeting with customers in the display industry to continue our constant dialogue about innovative solutions to meet the needs of the ever-changing high-tech market.”
Merck has a strong presence in the fast-growing emerging markets: aales in the region, which includes China, grew by 9% to around €3.8 billion last year, contributing 36% to group total sales of €10.7 billion in 2013.
Next month, groundbreaking is planned for Merck’s new €80 million (650 million Yuan) pharmaceutical manufacturing plant in the Nantong Economical Technological Development Area (NETDA), in the Greater Shanghai region (Yangtze River Delta area). Completion of the facility, which will focus on bulk production and packaging of Glucophage, Concor and Euthyrox, is scheduled for 2016, with commercial production starting in 2017. Merck’s brands for the treatment of diabetes, cardiovascular diseases and thyroid disorders are referenced in China’s Essential Drug List (EDL), making Merck the first and only multinational company in China to dedicate a large-scale green-field investment towards the production of drugs on the list comprising medicines that satisfy public healthcare needs and must be made available at all times.
In addition to investments in drug production, Merck has also expanded its services for biopharmaceutical R&D customers. Recent investments by the Merck Millipore life science tools business include the Biopharmaceutical Technical and Training Centre in Zhangjiang Hi-Tech Park, Shanghai. This center provides support, training and validation services to biopharmaceuticals customers with operations in China. The facility enables customers to investigate, explore and optimise their upstream and downstream processes, as well as environmental monitoring processes. In Beijing, where Merck Serono’s Chinese headquarters are located, Merck also runs a research center focused on biomarker research, including pharmacogenomics and bioanalytics, which is part of Merck Serono’s stratified medicine approach.
In addition to these investments, Merck counts on an extensive network of collaborations with leading academic and medical institutions in China, as well as local companies. The latest collaboration agreement with a Chinese company, announced in November 2013, is a second co-development and commercialisation agreement with BeiGene, which will further strengthen the companies’ collaboration in oncology.
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.