Device Safety and Vigilance
An introduction to the principles of adverse event reporting and risk assessment as applied to medical devices in the US, Europe, and other key international markets. The US has the most developed device vigilance processes but the course also summarizes the situation in Europe, Australia, Canada and Japan too. With coverage of risk assessment, AE report types, causality and event types, this course is designed to give a solid grounding in all key aspects of vigilance within this +$300 billion sector.
Average study time
Personal development points (CPD)
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GDvP- Device Safety & Vigilance
|1 x Licence||£79|
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- CPD Points - Gain Continuing Professional Development (CPD) Points, accredited by The Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. These can be used to count towards the distance learning element of any scheme that comes under the umbrella of The Academy of Medical Royal Colleges or any other scheme for which there is mutual recognition.
- Certification - Receive a personal certificate to show your subject knowledge on course completion.
- Affordable - You get excellent value through our cost-effective prices. We can also offer you group discounts on larger purchases.
- Flexibility - The course saves you time through the convenience of online availability. This lets you complete the interactive course at your own comfort.
- Keep Up to Date - You will stay up to date with any legislative changes in GCLP as our training courses are constantly monitored, reviewed and updated.
- Learn from Industry Experts - The course content has been developed to ensure that you comply with GCLP legislation through the application of learning outcomes. The course is written by Louise Handy, who is a past chairperson for the Research Quality Assurance (RQA)
*Interactive Courses contain over 70 unique mini-exams based on real-life cases to help learners apply their learning.