Tag archive

Updated

publicMedicines and Healthcare products Regulatory Agency (MHRA) · United Kingdom · Updated Aug 13, 2026

COVID-19 Test Approval: Introduction of CTDA Renewal Process and Portal

Manufacturers must submit renewal applications for CTDA certificates with a £420 fee (discounted to £168 for small organizations) and respond to any requests for additional information within 20 working days.

Country ComplianceRegulatory Intelligence Lead

SOP Impact1 SOPs

ConfidenceHigh

Relevant for: Regulatory Intelligence Lead, QPPV

verifiedRegulatory action: Guidance

Read impact briefarrow_forward

publicMedicines and Healthcare products Regulatory Agency (MHRA) · United Kingdom · Updated Aug 13, 2026

MHRA Update on MRI Equipment Safety Guidelines

Urgency: High

Clinical safety teams are required to review and implement the updated guidelines, ensuring that workflows for MRI equipment safety are compliant with the latest standards, particularly focusing on UKAS accreditation.

CAPARegulatory Intelligence Lead

SOP Impact1 SOPs

ConfidenceHigh

Relevant for: Regulatory Intelligence Lead, PV Quality Lead, QPPV

verifiedRegulatory action: Guidance

Read impact briefarrow_forward

Get updates for your PV role

Subscribe to impact-first pharmacovigilance updates. Select every role you want in your digest.

Digest roles: QPPV. Work email only