Hermann Schulze discusses the pre-clinical safety requirements that are expected to be conducted before a new molecular entity may be administered to human subjects.
Hermann Schulze discusses the pre-clinical safety requirements that are expected to be conducted before a new molecular entity may be administered to human subjects.
The first time a new molecular entity is administered to a human subject represents an important milestone for pharmaceutical companies,...
Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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A new pilot aims to take Brazil closer to ‘digital transformation.’
