Pharmaceutical Development Services & Analytical Testing Market Trends
Category Intelligence on Pharmaceutical Development Services & Analytical Testing covers the following
- Information relating to market, supply, cost, and pricing analysis
- Hard to find data on cost and TCO models, supplier details, and performance benchmarks
- Macroeconomic and regional trends impacting cost, supply, and other market dynamics
- Category-specific negotiation and sourcing advice
Industry Outlook & Drivers
Global Market Size and Growth Forecast –Pharmaceutical Development Services
- PDS accounts for about 5 percent of the total pharma R&D market. This market is estimated to increase from $7 billion in 2014 to $9.1 billion in 2018, seeing strong growth at a CAGR of around 5.5 percent, due to increased outsourcing by large pharmaceutical and biotechnology companies. This market is including both the large and small molecule development spend
- The Phase I/II PDS development market accounts 30 percent of the entire PDS global spending at $2.1 billion in 2014
Global Outsourcing Market Trend
- PDS outsourcing spend is expected to increase from $3.15 billion to $4.1 billion in 2018
- Outsourcing budgets have increased in recent years, swinging from contractions to expansion after the 2008 recession
- Pharma is maintaining its stance on outsourcing as a cost savings strategy
- Demands for biologics is a boon for contract manufacturing and contract research organizations
Growth Drivers and Constraints
Increased investment in R&D
- Increased investments at the discovery and early development phases are leading to robust pipelines and creating demand for greater clinical--scale manufacturing capacity.
Increase in biologic drugs
- The percentage of expenditure going towards biologics development and outsourcing expenditure have both risen over last year.
Broad array of services offering
- CDMOs are increasingly motivated to offer an expanded array of enhanced drug-delivery technologies, giving their customers broader options for patient care. Delivery technologies can include various targeted and timed release/dissolution and formulation technologies.
Increase in drug molecule complexity
- Drug molecules are becoming more complex and increasingly require both advanced synthesis and formulation expertise to realize cost-effective, efficacious medicines
Pressure of cost reductions
- The pressure on pharmaceutical firms to reduce costs was transferred to suppliers, which translated into reduced profit margins for suppliers.
Decline in number of initial public offerings (IPO)
- Without public markets, the industry could see a sharp drop in IND filings, and in the demand for CDMO services, as it did in 2010.
Increasing pharmaceutical In-house capability
- The pharma-biotech are investing significantly in internal manufacturing capabilities, through the expansion of existing or additional new manufacturing facilities and/or the acquisition of production capability