The US pharmaceutical market is forecast to increase from an estimated
value of $395.2 billion in 2014 to reach $548.4 billion by 2020, representing a
Compound Annual Growth Rate (CAGR) of 5.6%, according to new report.
The company’s latest report* states that this growth will be driven by
a number of factors, including increasing healthcare expenditure, an aging
population, the rising prevalence of chronic lifestyle diseases such as
diabetes and obesity, universal and easy access to reimbursement for
pharmaceutical product costs, and the 2010 Patient Protection and Affordable
Care Act (PPACA).
Publisher’s Director of Healthcare Industry Dynamics, explains that
the PPACA and its amendment, the Health Care and Education Reconciliation Act,
continue to have a substantial impact on US citizens and the country’s
pharmaceutical industry.
Publisher’s Director says: “As the PPACA mandates health insurance
coverage for all Americans, the US has witnessed increasing use of prescription
drugs among individuals who are newly insured or have shifted to insurance
plans that offer premium and cost-sharing subsidies. In 2014, spending on
prescription drugs amounted to an estimated $275.9 billion, compared with $262.3
billion in 2013.
“Around 20 provisions of the healthcare legislation are expected to
have a direct or indirect impact on the volume of drug and biologic sales. As
many as 32 million formerly uninsured citizens could enter the patient pool,
resulting in new business worth $115 billion over a period of 10 years.”
Publisher’s report also notes that the US Food and Drug Administration
(FDA) provides a transparent, well-structured and competent regulatory system
to facilitate the approval of pharmaceutical products and consequently bolster
market growth.
Publisher’s Director continues: “New initiatives undertaken by the FDA
to strengthen the review and approval process will be advantageous to the
industry. Its strong patent system attracts research-based pharmaceutical
companies and positively influences growth.
In 2014, 41 novel drugs were approved by the FDA, 17 of which were for
the treatment of rare diseases. Schemes such as the FDA’s Fast Track
Development Program and Breakthrough Designation accelerate the approval of
novel drugs and add value to the market by meeting demand more quickly.
CountryFocus: Healthcare, Regulatory and Reimbursement Landscape - US
report provides information on the healthcare, regulatory, and reimbursement
landscape in the US. It includes an overview of the pharmaceutical and medical
device sectors, including market size, segmentation, and key drivers and
barriers, as well as annualized revenue data from 2013 and forecast to 2020.
This report was built using data and information sourced from
proprietary databases, primary and secondary research, and in-house analysis
conducted by Publisher’s team of industry experts.
For
further information on this report, please visit- http://mrr.cm/4fL
Find all Healthcare Reports at: http://www.marketresearchreports.com/healthcare
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