It's a common problem - there is never enough space to fit everything you want onto medicinal packages. With the pressures of compliance increasing, future regulations such as IDMP and Serialization will require that even more data is presented on each label.
Werum and EXTEDO have partnered to ensure that PAS-X and RImanager have the answers to your pains. During our session at Werum's forthcoming user group meeting, EXTEDO will demonstrate how technology provides essential bridge between the world of regulatory submissions and the need for manufacturing implementation.
If you're not already registered, then register online now.
The Bridge Between Regulatory Submission Management and Manufacturing Implementation
What we will cover
- Discussion how to manage regulatory product packaging
- How technology solutions improve processes and data quality
Who should participate?
- Regulatory Affairs Managers, Head of Manufacturing, Directors, VPs
- IT / Business-IT Managers, Chief Information Officers
Event Details and Registration
Friday, 02 December 2016
08:30 h - 10:00 h CET (Madrid, Berlin)
Bei der Lüner Mühle
Participation is free of charge