Technical documentation according to MDR (EU)
WHEN
From: 31. May 2023
To: 01. Jun 2023
WHERE
Helsinki, Finland
LANGUAGE
The training will be conducted in Finnish
COST
1190 € (+ VAT)
Register
Contact us to enquire about this session
SGS Academy in Finland is conducting for Medical Device manufacturers, importers and distributors a two-day training:
In this training you will hear how the requirements of technical documents and the creation of documentation for e.g. electrical safety, biocompatibility, Medical Device cleanliness and sterilization can affect the operation in your own company.
Training is conducted in Finnish.
Technical Documentation According to MDR (EU), Biocompatibility, Medical Device Cleanliness and Sterilization Requirements, and Clinical Evaluation
Date and location: May 31st and June 1st 2023 9 am – 4:30 pm (Registration and breakfast starting 8.40 am) Juju Kampus, Takomotie 8, 00380 Helsinki
The European Medical Device Regulation MDR (EU) 745/2017 replaces the Medical Device Directive (MDD) 93/42/EEC on May 26, 2021. It applies to all EU countries, all device manufacturers, device importers and distributors.In this training you will hear how the requirements of technical documents and the creation of documentation for e.g. electrical safety, biocompatibility, Medical Device cleanliness and sterilization can affect the operation in your own company.
Training is conducted in Finnish.