Commission will accept comments on recent workshop, eight identified weight-loss ad claims through Feb. 3. During Strategic Research Institute conference Dec. 9, Division of Advertising Practices Senior Staff Attorney Richard Cleland noted that after comment period closes, FTC will put together staff report with recommendations on whether eight claims are scientifically feasible, as well as suggestions on industry self-regulation, media screening of weight-loss ads. November workshop featured scientific panel that almost unanimously concluded eight weight-loss claims, such as "works for everyone," lack sufficient scientific support (1"The Tan Sheet" Nov. 25, 2002, p. 4)...
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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.’
The European Medicines Agency’s chief medical officer Steffen Thistrup argued that patients are able to understand the “complex regulatory and scientific issues” that the EMA committees discuss when they assess drugs.
Monitoring the use of decentralized elements in clinical trials is a priority for the European medicines regulatory network.
Pfizer told the Pink Sheet it would work with the health technology assessment institute, NICE, with the hope of making Hympavzi available to patients with hemophilia A via the National Health Service.
