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Home » Newsletters » BioWorld

BioWorld

Nov. 3, 2010

View Archived Issues

FDA Hears Complexities of Biosimilar Implementation

SILVER SPRING, Md. – The FDA Tuesday began facing some of the complexities it must deal with in developing regulations and guidelines for makers of follow-on biologics, or biosimilars, as various stakeholders in eight-minute presentations at a public meeting spelled out some of their ideas and concerns, such as whether biosimilars should carry the same generic-type name, known officially as the international nonproprietary name (INN), as the innovator drugs on which they are based. (BioWorld Today) Read More

FDA, EMA Filings in 2011 if Linaclotide Data are Positive

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Ghostwritten Articles: Tail that Wags Off-Label Drug Promos

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NewCo News: Multiplatform Taiga Scores NIH Funding for HSC Technologies

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From Microneedles to Water Buffalo: Studies in Collaboration

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Stock Movers

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Clinic Roundup

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Financings Roundup

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Other News To Note

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