Global Pharmaceutical Contract Development and Manufacturing Market report from Global Insight Services is the single authoritative source of intelligence on Pharmaceutical Contract Development and Manufacturing Market. The report will provide you with analysis of impact of latest market disruptions such as Russia-Ukraine war and Covid-19 on the market. Report provides qualitative analysis of the market using various frameworks such as Porters’ and PESTLE analysis. Report includes in-depth segmentation and market size data by categories, product types, applications, and geographies. Report also includes comprehensive analysis of key issues, trends and drivers, restraints and challenges, competitive landscape, as well as recent events such as M&A activities in the market.
Pharmaceutical Contract Development and Manufacturing (CDMO) is a process by which a company outsources the development and manufacturing of a new drug or other pharmaceutical product to another company. The CDMO industry has grown in recent years as more and more pharmaceutical companies seek to focus on their core competencies and outsource non-core activities.
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Key Trends
The pharmaceutical industry is facing a number of challenges that are driving the need for new and improved contract development and manufacturing technologies. These challenges include the need to improve product quality, reduce costs, and increase manufacturing efficiency.
One of the key trends in pharmaceutical contract development and manufacturing technology is the use of continuous manufacturing processes. Continuous manufacturing is a manufacturing process in which products are produced in a continuous flow without interruption. This type of manufacturing can improve product quality and reduce costs by reducing the amount of time and materials required for production.
Another trend in pharmaceutical contract development and manufacturing technology is the use of advanced analytical techniques. These techniques can help to improve product quality by providing more information about the products being manufactured. Additionally, these techniques can help to reduce costs by providing information that can be used to improve manufacturing processes.
Key Drivers
The global pharmaceutical contract development and manufacturing market is driven by the outsourcing of clinical trials and drug development by pharmaceutical and biotechnology companies. The outsourcing of these activities to contract research organizations (CROs) and contract manufacturing organizations (CMOs) enables pharmaceutical companies to focus on their core competencies, reduce costs, and speed up the drug development process. The increasing number of FDA-approved drugs and the growing number of orphan drugs are also driving the market. In addition, the increasing number of mergers and acquisitions in the pharmaceutical industry is expected to drive the market.
Market Segments
The Pharmaceutical Contract Development and Manufacturing Market is segmented based on type of contract manufacturing, end user, and geography. Based on type of contract manufacturing, the market is segmented as, Active Pharmaceutical Ingredients (API) / Bulk drug, Final Dosage Form (FDF), advanced drug delivery products, OTC medicines and Nutritional products and Packaging contract manufacturing. By end user, it is divided into big pharmaceutical companies, small and medium-sized pharmaceutical companies, generic pharmaceutical companies and others. Region-wise, it is studied across North America, Europe, Asia-Pacific, and the Rest of the World.
Key Companies
Top key players in Pharmaceutical Contract Development and Manufacturing Market are Thermo Fisher Scientific Inc, Catalent, Inc, Lonza Group Ltd., Recipharm AB, Vetter Pharma International GmbH, FAMAR Health Care Services, AbbVie Inc, Aenova Group, Almac Group, Siegfried Holding AG, Evonik Industries AG , WuXi AppTec, and Samsung BioLogics.
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