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Pharma Mergers: FTC Should Consider Monitoring R&D, Assessing PBM Contracts, Experts Advise

 
• By Brenda Sandburg

Panelists at FTC/DOJ workshop suggest new remedies to ensure pharma mergers are not anti-competitive. The commission should support scientists and ensure R&D continues, one expert says.

M&A
Pharmaceutical mergers may face new hurdles in getting US FTC clearance • Source: Shutterstock

The US Federal Trade Commission and Department of Justice should look at the past conduct of pharma companies seeking to merge, including their contracts with pharmacy benefit managers, and monitor the outcome of a merger on research and development, experts advised the agencies.

In the first day of a virtual two-day workshop on pharmaceutical mergers, panelists discussed factors the FTC should consider in...

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• By Eliza Slawther

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EU Emergency Response Authority Needs Bigger Budget To Address Health Threats, Says Industry

 
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The EU must renew the mandate of its Health Emergency Response Authority to support medicine stockpiles and enable agile manufacturing to combat antimicrobial resistance and chemical, biological, radiological and nuclear threats, says trade organization EUCOPE.

How Pharma Companies Can Mitigate The Impact Of US Tariffs On The Supply Chain

 
• By Ewan Townsend

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Semaglutide: EMA Safety Probe Confirms Rare Eye Disorder Risk

 
• By Neena Brizmohun

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Infographic: Leqembi – A Geographical Comparison

 
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EU Pharma Reform: Council Proposal A ‘Step In The Right Direction’ But ‘More Work To Be Done’

 
• By Eliza Slawther

Experts from EUCOPE explain why the Council of the EU’s position on the proposed overhaul of the general pharmaceutical legislation could offer more predictability for companies than the commission’s initial offering.