Online Performance Evaluation & Post-Market Surveillance on Medical Devices & IVD’s Under MDR & IVDR
Registration is now closed for this training course. Please contact jasmin@onenucleus.com to be added to the waitlist.Online Performance Evaluation & Post-Market Surveillance on Medical Devices & IVD's Under MDR & IVDR |
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| Audience |
Knowledgable on Medical Devices industry areas such as: Research & Product Development, Regulatory Affairs and Quality Management. |
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| Duration |
A two day online course on Microsoft Teams. Timings below for both days: 9.00-12.10: Session One (Q&A and breaks integrated) 12.10-13.00: Lunch Break 13.00-14.40 Session Two (Q&A and breaks integrated) |
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| Objectives |
To give the regulatory prospective and practical insight on the following areas: - Performance Evaluation Requirements for MDs /IVDs under MDR/IVDR - Post-Market Surveillance and Post-Market Clinical follow up requirements for MDs /IVDs under MDR/IVDR |
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| Costs |
Gold Members: £234.50 + VAT |
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This training course will be delivered by PLG (ProductLife Group). ProductLife Group’s mission is to improve human health by delivering regulatory compliance services for the safe and effective use of medical solutions.
For almost 30 years, PLG has supported clients through the entire product life cycle, combining local expertise with global reach spanning more than 140 countries. It provides consulting and outsourcing services in the areas of regulatory affairs, quality and compliance, market access (pricing & reimbursement), vigilances and medical information, covering both established products and innovative therapeutics & diagnostics.
With a goal of continuously improving the value delivered to people and customers, PLG is committed to long-term partnership, innovation, flexibility, and cost efficiency.
For more information, visit productlifegroup.com.
Cambridgeshire
United Kingdom