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About Neena


34+ years of experience

Neena has over 20 years of experience covering regulatory, business and market access developments impacting pharmaceutical and medical device companies. She explores the challenges and opportunities that developments worldwide introduce for industry and regulators. Her areas of expertise include regulatory schemes for getting products to market faster.

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.

Analyst Articles

Articles by Neena