"HARMFUL HERBS" REVIEW BY U.N.-SPONSORED EXPERT PANEL suggested in a draft report of the Codex Committee on Nutrition and Foods for Special Dietary Uses Oct. 7-11 meeting in Bonn, Germany. Asked by the Codex Executive Committee to consider the implications of a Canadian delegation paper addressing "potentially harmful herbs and botanical preparations sold as foods," the nutrition/special dietary uses committee determined that the group lacks the necessary experience to deal with the issue. The Canadian paper suggested that lists of "positive" and "negative" botanical ingredients be developed.
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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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A new pilot aims to take Brazil closer to ‘digital transformation.’
Germany’s federal health care decision-making body, the G-BA, tells the Pink Sheet that German drug prices are fair and speculation of price rises in the market due to the US MFN policy is fear mongering.
EU marketing applications for drugs aimed at slowing myopia progression in children and for treating cutaneous T-cell lymphoma have been turned down by the European Medicines Agency.
The verdict by the Unified Patent Court in the dispute between Sanofi/Regeneron Pharmaceuticals and Amgen explains what companies should look out for when deciding whether infringement has taken place when it comes to second medical use patents.
