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UK Casts Wider Net With Pfizer/BioNTech’s COVID-19 Vaccine

Longer Time Lag Between Two Doses Will Maximize Vaccination Outreach

 
• By Vibha Sharma

The UK MHRA has crunched the safety and effectiveness data on the Pfizer/BioNTech COVID-19 vaccine and permitted its use by even more people.

Trailer truck delivering covid-19 vaccine
UK Wants To Vaccinate As Many People As Possible In Face Of Growing COVID-19 Cases • Source: Shutterstock

The UK medicines regulator has expanded the use of Pfizer/BioNTech’s COVID-19 vaccine in women who are pregnant and breastfeeding when beneficial, and in people with known allergies. It has also made changes to the vaccine’s dosing interval - allowing a potentially longer time gap between the two doses that need to be administered.

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HRA To Revisit Simplified Consent Provisions Under New UK Clinical Trials Law

 
• By Vibha Sharma

Study sponsors looking for guidance on how the simplified informed consent provisions will be implemented under the new UK clinical trials legislation will have to wait longer. The Health Research Authority is looking at what safeguards are needed to address the “range of concerns” stakeholders had regarding its initial proposal.

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UK Promises To ‘Turbocharge’ Clinical Trials As US Tariff Threat Remains

 
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Trump’s Tariffs Will Lead To ‘Instability’ And ‘Less Investment’ In UK

 
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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.

More from Europe

Leqembi Launch Set For Germany & Austria After Winning EU Approval At Last

 
• By Neena Brizmohun

Eisai is working on securing reimbursement across the EU for Leqembi now that the Alzheimer’s disease treatment has secured marketing approval from the European Commission.

EMA Initiative To Address Information Overload In CTIS Training Materials

 
• By Vibha Sharma

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HRA To Revisit Simplified Consent Provisions Under New UK Clinical Trials Law

 
• By Vibha Sharma

Study sponsors looking for guidance on how the simplified informed consent provisions will be implemented under the new UK clinical trials legislation will have to wait longer. The Health Research Authority is looking at what safeguards are needed to address the “range of concerns” stakeholders had regarding its initial proposal.