Office of Dietary Supplements urged to "continue and expand" research initiative on ephedra safety and efficacy under Senate appropriations bill passed Oct. 11. ODS, NCCAM have commissioned an AHRQ study on ephedra, which could be released as early as August 2002 (1"The Tan Sheet" Aug. 13, p. 10). Appropriations bill also urges ODS to "allocate sufficient funds to expand the number of botanical research centers," with hypericum, echinacea suggested subjects of study. Bill would allocate NCCAM $110 mil. for FY 2002 (2"The Tan Sheet" Oct. 15, In Brief)
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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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While the first six months of the year saw eight new drugs targeting a range of diseases enter the European Medicines Agency’s priority medicines scheme, and three PRIME-designated treatments go on to win EU marketing approval, use of the accelerated assessment mechanism appears to be limited.
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