Connecting Regulatory and Production Processes - Unravelling Medicinal Packaging Regulations

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.

Session Details

The Bridge Between Regulatory Submission Management and Manufacturing Implementation

What we will cover

  • Introduction
  • 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

Date:

Friday, 02 December 2016

08:30 h - 10:00 h CET (Madrid, Berlin)

Location:

Hotel Bergström

Bei der Lüner Mühle

21335 Lueneburg

Germany

 

Participation is free of charge

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