Clearing the way for transparency in drug regulation
This article was originally published in SRA
Transparency is everything – or so it would appear. Barely a week goes by without new proposals to put more information into the public domain, set new conditions for experts sitting on advisory committees, or limit companies' freedom to hand out gifts.
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A list of EU biosimilar filings, CHMP opinions and EU marketing authorizations, including details of the biosimilar company, the brand name/INN, indication(s), the reference product/company, and the date and type of event.