Neena Brizmohun
Deputy Editor
UK
+34 year(s) experience
Neena's other specialist areas include new medicines coming to market in the EU, clinical trials, post-marketing safety monitoring, transparency policies relating to the publication of trial data, and global harmonization initiatives for pharma and medtech.
A scientist by training, Neena started her journalistic career at Informa in 1997. Before becoming a journalist she worked as a biomedical scientist at St Thomas' Hospital in London for 10 years.
Pink Sheet: 世界の薬事規制と承認審査に関するニュース
Joining the international regulatory collaboration could become a key route for the UK to remain an early and priority market for global launches after the end of the Brexit transition period, says the industry group, BIA.
Topic Pharma-Brexit brexit
Pink Sheet: 世界の薬事規制と承認審査に関するニュース
The regulatory agency also urges qualified persons at drug companies to let the agency know as soon as possible if they are finding that the new measures are not flexible enough to deal with the current logistical challenges quickly.
Pink Sheet: 世界の薬事規制と承認審査に関するニュース
The stakes are extremely high for companies called before EU or US regulators and scientific experts to answer queries about their new drug applications at the later stages of the review process. How they perform is critical. Consultant Kate Dion has a raft of helpful tips for companies facing this daunting situation. Neena Brizmohun reports.
Topic drug-approval
Pink Sheet: 世界の薬事規制と承認審査に関するニュース
Novartis, having now submitted its CAR-T therapy CTL019 to the European Medicines Agency for approval.
Topic drug-review
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