EMA rewrites medicine approval policy

New innovative medicines should be made available to European citizens more quickly. That is why the European Medicines Agency updates the process for market authorisation. Anthony Humphreys sighs when asked what the new strategy means for doctors. ‘What can I possibly say?’ The former pharmacist from Ireland is responsible for EMA’s ‘Regulatory Science to 2025’ …

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NVWA barely has grip on tobacco industry

Violations of the advertisement ban by tobacco manufacturers are seldom noticed by inspection authorities. That is the conclusion of The Investigative Desk after analysing ten years of inspections carried out by the Netherlands Food and Consumer Product Safety Authority (Nederlandse Voedsel- en Warenautoriteit, NVWA). The agency also regularly loses out in their juridical test of …

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