On 4 February the Gabinete Técnico Farmacéutico M. Camps and consultancy Azierta organise the webinar "Vigilance and post-marketing of medical devices".
This training, which will be held online for registered users -attendance is free of charge, subject to registration- will provide an overview of regulation and the steps to be taken to carry out PS monitoring.
The market surveillance and monitoring are an essential part of the marketing of medical devices.This is a sector in continuous innovation and of great importance in the European and Spanish market.
The webinar will be moderated by:
- Mercè Camps. CEO and founder of the Technical Pharmaceutical Cabinet MCamps
- Olegario Cuevas. Healthcare Business Manager at Azierta
The webinar presentation will be conducted by:
- Silvia de Andrés. Medical Devices Officer
- Alberto Orós. Technical Consultant
Surveillance and marketing of medical devices:
webinar programme
-
-
- Introduction
- Surveillance system
- Incident management
- Security corrective actions (FSCA) and security notices (FSN)
- Trend reporting
- Post-market surveillance system
- Periodic Security Update Report (PSUR)
- Post Market Monitoring Report (PMSR)
- Post-marketing clinical follow-up
-
Latest articles in our blog
International Meeting on Health Regulation: 5th edition of the intercontinental congress on health regulation
5th International Meeting on Health Regulation: GTF's director, Mercè Camps, participates in a round table on the regulation of Medical Devices and CE Marking.
Probiotics: AESAN updates its criteria on food supplements
Probiotics are part of many food supplements.
RistarLab: Mercè Camps visits the facilities of a food supplement manufacturer‘
At its industrial plant in Ripollet (Barcelona), RistarLab offers a wide range of services aimed at the manufacture and formulation of food supplements and food products.