PV Bulletin

Role

Medical Device Vigilance Lead

Device Vigilance Leads manage post-market surveillance distinct from medicinal product pharmacovigilance yet increasingly interconnected. Monitor FDA device recalls, field safety notices, MDR vigilance obligations, and drug–device combination updates requiring coordinated safety assessment across PV and quality teams.

7 updates · Sorted by impact priority

publicFda · United Kingdom · Updated May 24, 2026

MHRA updates SaMD/AIaMD guidance, highlighting PCCP and transparency principles

Urgency: High

Ask the safety/device vigilance and PV CSV leads to: (1) confirm whether any marketed/fielded SaMD/AIaMD uses adaptive ML or planned updates that would fit a PCCP-like approach; (2) review current change-control SOPs and technical documentation to ensure change governance and transparency artifacts are captured and retrievable; (3) verify post-market/vigilance processes explicitly account for algorithm updates (e.g., monitoring after updates, escalation criteria).

Risk ManagementDevice VigilanceSignal Management Lead
SOP Impact5 SOPs
ConfidenceMedium
Relevant for: Signal Management Lead, Regulatory Intelligence Lead, Medical Device Vigilance Lead
verifiedRegulatory action: AI/GxP
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publicMhra · United Kingdom · Updated May 24, 2026

MHRA hub consolidates GB medical device PMS, MORE reporting and PSUR

Urgency: High

Safety/Device Vigilance owner to: (1) confirm SOPs and training link to MHRA’s “Medical devices: post-market surveillance” collection as the live index; (2) validate operational readiness to submit adverse incident and FSCA-related reports via MHRA’s referenced MORE route; (3) confirm device PSUR process uses MHRA-linked standardised PSUR format and PSUR guidance tied to the Regulations 2024 framework; (4) update internal regulatory intelligence trackers with the 16 June 2025 in-force date cited across MHRA guidance, and monitor related MHRA future regime pages for further updates.

Local Affiliate ComplianceDevice VigilanceLocal Safety Officer
SOP Impact6 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Regulatory Intelligence Lead, PV Operations Lead
verifiedRegulatory action: Country Guides
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publicFda · Updated May 22, 2026

FDA ties TRUE METRIX Safety Communication to Class I recall update

Urgency: High

Fda update requires triage for Signal Validation, Local Affiliate Compliance, Device Vigilance; confirm local obligations and document follow-up actions.

Signal ValidationLocal Affiliate ComplianceLocal Safety Officer
SOP Impact7 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Signal Management Lead, Regulatory Intelligence Lead
verifiedRegulatory action: Regulators
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publicFda · Updated May 22, 2026

FDA MDR hub highlights VMSR guidance and quarterly malfunction reporting

Urgency: High

Fda update requires triage for Local Affiliate Compliance, ICSR Submission, Device Vigilance; confirm local obligations and document follow-up actions.

Local Affiliate ComplianceICSR SubmissionLocal Safety Officer
SOP Impact4 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Regulatory Intelligence Lead, PV Operations Lead
verifiedRegulatory action: Devices
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publicHealth Canada · Updated May 22, 2026

Health Canada reposts device recall forms and updates GVP GUI-0102

Urgency: High

Health Canada update requires triage for Local Affiliate Compliance, Device Vigilance, Inspection Readiness; confirm local obligations and document follow-up actions.

Local Affiliate ComplianceDevice VigilanceLocal Safety Officer
SOP Impact4 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Regulatory Intelligence Lead, Medical Device Vigilance Lead
verifiedRegulatory action: Regulators
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publicMhra · Updated Apr 29, 2026

MHRA issues April 2026 Safety Roundup for medicines and devices

Urgency: Medium

Mhra update requires triage for Signal Validation, Local Affiliate Compliance, Device Vigilance; confirm local obligations and document follow-up actions.

Signal ValidationLocal Affiliate ComplianceLocal Safety Officer
SOP Impact5 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Signal Management Lead, Regulatory Intelligence Lead
verifiedRegulatory action: Devices
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publicTga · Australia · Updated May 24, 2026

Australia: TGA refreshes device post-market monitoring hub and responsibilities

Monitoring

1) Add/confirm the TGA 'medical device post-market monitoring and safety updates' page as a tracked regulatory intelligence source for routine review. 2) Cross-check internal Australia device vigilance SOPs/work instructions against TGA guidance on sponsor/manufacturer post-market responsibilities and document any gaps for CAPA/change control as needed.

Signal ValidationLocal Affiliate ComplianceLocal Safety Officer
SOP Impact5 SOPs
ConfidenceMedium
Relevant for: Local Safety Officer, Signal Management Lead, Regulatory Intelligence Lead
verifiedRegulatory action: Devices
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