Medical Device Post-Market Surveillance and Vigilance: Complaints, Trends and Field Actions – London, 11–15 Jan 2027
Medical Device Post-Market Surveillance and Vigilance: Complaints, Trends and Field Actions runs in London from Monday 11 January to Friday 15 January 2027 (1 Week). The fee is 23,000 SAR per participant. The same programme is also scheduled in 7 other cities.
- Dates
- Length
- 1 Week
- Fee per participant
- 23,000 SAR
- Format
- In person, London
- Venue
- Central London four-star
- Status
- Open for registration
- Week
- 2 of 2027
- Reference
- 469_14393
This session
11–15 Jan 2027
This Medical Device Post-Market Surveillance and Vigilance: Complaints, Trends and Field Actions session in London runs from Monday 11 January to Friday 15 January 2027 (week 2, Q1 2027). It is the 1st of 2 dates in London in 2027, at a fee of 23,000 SAR, the same for each of them. Registration is open for this date. It is held in person at Central London four-star.
When else does it run in London?
- 11 – 15 January 2027 This date 23,000 SAR
- 16 – 20 August 2027 23,000 SAR
How do I book this date?
Register online to request your place, or send us a question about this date first.
Reference for this date: 469_14393. Quote it when you contact us.
Before you book, read our cancellation policy.
Let’s talk about your next step.
Questions about this date
When does Medical Device Post-Market Surveillance and Vigilance: Complaints, Trends and Field Actions in London start and finish?
It starts on Monday 11 January and finishes on Friday 15 January 2027: 1 Week.
How much does Medical Device Post-Market Surveillance and Vigilance: Complaints, Trends and Field Actions in London cost?
The fee for this date is 23,000 SAR per participant. Please read our cancellation policy before you book.
Is this date held in person or online?
It is held in person in London, at Central London four-star.
What does this programme cover?
Medical device post-market surveillance breaks down when complaints sit in customer service logs, service reports never reach quality, trends are spotted only after several patients are affected and nobody can say quickly whether an event must be reported. This Core Concept course trains regulatory affairs, quality, complaint handling and distributor staff to run a proactive surveillance system for medical devices and IVDs, from data collection and complaint investigation to signal detection, incident reporting, field safety corrective actions and periodic safety reports. Participants produce a Post-Market Surveillance Plan and Vigilance Decision Pack.
The programme outline covers:
- Introduction
- Course Objectives
- Target Audience
- Course Outline
- Day 1: Post-Market Surveillance Purpose, Roles and Data Landscape
- Day 2: ISO/TR 20416, ISO 13485 Feedback Clauses and IMDRF Terminology
- Day 3: Complaint Investigation, Trend Analysis and Signal Detection
- Day 4: Reportable Incidents, Field Actions and Periodic Reporting
- Day 5: Case Study Workshop: Surveillance Plan and Vigilance Decisions
- Skills You Will Gain
- Why Attend This Course
- Conclusion
Where else does this programme run?
Also scheduled in 7 other cities.
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