Three-way talks among the EU institutions on a new fee structure at the European Medicines Agency are expected to begin in September after the European Parliament adopted amendments to a draft regulation that will base fee levels more closely on the actual costs of regulatory work performed by the EMA.
EMA Fee Proposals Pass Another Legislative Milestone
Agreement on a new, more streamlined fee structure for the European regulator could be reached by the end of this year.

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While the pharma industry appears to be exempt from US tariffs imposed by President Trump, a member of the UK House of Lords says the details are unknown and warned that uncertainty “leads to less investment” in business as a whole.
The EU Clinical Trials Information System has achieved primary registry designation in the International Clinical Trials Registry Platform in a move that is expected to reduce regulatory burden for companies and help them lower compliance costs by aligning with publication requirements in medical journals.
The UK government has listened to industry concerns about high clawback rates under the voluntary scheme and will review it in June in a bid to resolve the issue and “move on to bigger and more important things,” health secretary Wes Streeting says.