CPSC CRP TESTING LESS LIKELY WITH COMPANY DATA ON FILE, Consumer Product Safety Commission Project Manager Suzanne Barone, PhD, said at a Feb. 13 Nonprescription Drug Manufacturers Association and Pharmaceutical & Medical Packaging News workshop in Somerset, N.J. Noting that CPSC has "limited funds" for testing marketed child-resistant packaging, Barone explained that companies that voluntarily submit their own passing CRP data to CPSC are not likely to be subject to commission testing unless difficulties come to light through consumer complaints or adverse events.
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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.’
Sarepta's rAAVrh74 vector, used in the marketed Duchenne muscular dystrophy gene therapy Elevidys and across the company's limb girdle muscular dystrophy pipeline, earned a platform designation as the lead LGMD candidate prepares for BLA filing.
Pink Sheet reporter and editors discuss the potential impact of the Most-Favored Nation drug pricing proposal on Europe, the United States, as well as the pharmaceutical industry.
Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.
