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PharmaForce International: Post-Approval Biosimilar Drugs Encounter Obstacles When Entering into the US Market


READING, Pa., Dec. 10, 2019 /PRNewswire/ -- PharmaForce International's recent syndicated report benchmarks leading Biosimilar sales and marketing organizations in the United States. This study profiles various biosimilar products competing in high-demand markets such as Oncology, Immunology, and Diabetes. One key finding is the delay of select biosimilar products in entering the vastly competitive market. A few leading companies have experienced lengthy hold-ups in launching their biosimilar products.

The report identifies several noteworthy developments as to why these Biosimilar products are facing such barriers. One reason, in particular, is due to the reactive contracts of reference products. The companies promoting these reference products have formed innovative contracting tactics with hospitals to defend their share of the market.

Joyce Wedemeyer, Director of Sales and Marketing at PFI, says "The effective contracting strategies and competitive discounting of reference products are major contenders in the postponement of successful launches of Biosimilar products."

"Companies need time to strategically coordinate the market-entry of their biosimilar products to ensure they meet industry expectations" says Wedemeyer

The report includes more granular insights, which will enable clients to:

For more information on the report mentioned above, please contact Joyce Wedemeyer at [email protected] or by phone at 610-370-2906.

PharmaForce International (PFI) is a competitive intelligence firm with over two decades of experience in the pharmaceutical and biotech industries. PFI has become the market leader in commercial operations benchmarking and competitive intelligence.

Related Links https://www.pharmaforce.biz

SOURCE PharmaForce International


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