Welcome to PREVENTIA. We prevent errors.
PREVENTIA focuses on Quality Assurance and Regulatory Affairs consulting and training within the Medical Device and Pharmaceutical Industry.
We assist organizations to prevent errors through qualified training and education in Quality and Risk Management.
As trainers we offer professional and motivating training with high learning-efficiency.
As consultants we create long term engagement with extreme service that leads to permanent results.
We offer a net-work of consultants with high competency and we always do our outmost to exceed your expectations on training and consultancy services.
PREVENTIA AB is located in Bjärred outside of Malmö in the south of Sweden.
SE 237 36 BJÄRRED
PREVENTIA offers a network of proffessional consultants to serve you in the best possible way!
Sterilization of Medical Devices – a one week ten credit course in the different sterilization techniques, a written examination last day, next course in November 18 – 22, 2019, China. questions – firstname.lastname@example.org
Sterilization of Medical Devices – a one week ten credit course in the different sterilization techniques, a written examination last day, coming course in May 11 – 15, 2020 Malmö, Sweden. questions – email@example.com
ISO 13485:2016 and the Practical Guide for ISO 13485 Be programme – To give an understanding of the changes, why we have made the changes and also give guidance how to implement the changes. The main focus is on the changes, but the full standard will be covered although not all parts so detailed as the changed parts. We also give the full course for beginners! Questions – firstname.lastname@example.org
The MDR, Medical Device Regulation, released May 2017. Programme; the new MDR and the implications for industry. Education occasions – questions; email@example.com
Coming (2019?) ISO 14971 Risk Management and the TR 24971 Guidance for Risk Management;questions; firstname.lastname@example.org
Other Courses see;
Medical Device Regulation: https://www.dnvgl.dk/training/medical-device-regulation-156023
ISO 13485: https://www.dnvgl.dk/training/iso-13485-2016-156033
Risk Management ISO 14971: https://www.dnvgl.dk/training/risk-management-iso-14971-2012-incl-updates-on-the-fdis-14971-2019-and-24971-2019-156034
Post Marketing Surveillance: https://www.dnvgl.dk/training/post-market-surveillance-156037
Clinical Evaluation Report: https://www.dnvgl.dk/training/clinical-evaluation-report-156036