- TypeWebinar
- Location San Jose, California, United States
- Date 22-04-2021
Engineering
Administration/Management
Architecture/Interior Designing
Medical/Healthcare/Hospital
This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2019 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, EU Directive 93/42/EEC on Medical Devices.