A new AI capability that delivers analysis-ready Media Intelligence. More than just a product launch, this is a shift in how communications teams monitor, understand and act on media coverage.
Deputy editor of Pink Sheet/Scrip/Medtech Insight. Interested in science, pharma and medtech. All views expressed are my own.
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile
Get in touch with Neena
Contact Neena, search articles and posts on X, monitor coverage, and track replies from one place.
As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
The verification pathway, which took effect this month, is designed to speed up drug approvals by relying on marketing approvals from regulators in Australia, the US, Canada, the UK, the EU, Singapore and Switzerland.
Increasing alignment and coordination on topics related to medicines is among the deliverables in a working arrangement signed by the European Commission, the European Medicines Agency and the New Zealand Ministry of Health.
The European Directorate for the Quality of Medicines & HealthCare has aligned a raft of EU guidelines on official control authority batch release with the European Pharmacopoeia Commission’s strategy to phase out the rabbit pyrogen test.