Eastern Europe's pharmaceutical market is forecast to grow at a CAGR of more than 10% to be worth more than $41 billion by 2014, according to a report from companiesandmarkets.com.
Eastern Europe's pharmaceutical market is forecast to grow at a CAGR of more than 10% to be worth more than $41 billion by 2014, according to a report from companiesandmarkets.com. The highest sales are expected to be seen in the cardiovascular market ($7.8 billion), followed by alimentary canal and metabolic disorders ($6 billion).
According to the report, The Eastern European Pharmaceutical Market Outlook to 2014, the main player in the region is Novartis, which led the market with $1. 5 billion in sales in 2007 thanks to the marketing of both generic and branded pharma products. However, the leading treatment in 2007 was sanofi-aventis' Lovenox (enoxaparin) with sales of $152 million.
Traditionally, pharma companies have been quite successful in Eastern European countries; however, healthcare systems have become increasingly complex during the past few years. As a solution, governments have been attempting to reduce costs by launching healthcare reforms. Many countries have now introduced regulated health insurance systems to replace state-controlled healthcare, and the Czech Republic and Slovenia have also opened up health insurance markets to competition from private insurers.
This move to curb pharmaceutical expenditure could lead to new opportunities for pharma companies involved in the manufacture of generics. According to the report, niche players tend to perform well in the region; for example, Krka (Slovenia) led the Slovenian market in 2007 with the generic gastrointestinal OTC product Ultop. The move to reduce drug expenditure may also drive the acceptance of biosimilars. Initially, well-established generic manufacturers with advanced development programmes are expected to perform well, but small- to medium-sized biopharm companies are also expected to emerge in the longer-term.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.