INFOTEHNA at Regulatory (e)Document Management Conference
January 30, 2012 - Pullman Berlin Schweizerhof, Berlin, Germany
Join INFOTEHNA at the conference on the most pressing pharmaceutical issue - From (e)Document Management to Information Management
Pharmaceutical companies are subject to a variety of complex regulations, which they must meet every day. To create, maintain, manage and archive myriad of documents specific document and information management solutions are required.
Among the speakers, that will present their views on the issue, will be Stefan Horneborg, Principal Sales Manager in INFOTEHNA GmbH.
Listen to Mr. Horneborg's presentation: Global Compliance with integral Document Management System on January 30, 2012 at 12:00. Synopsis of the presentation:
- from Document to Management
- from Research & Development to pharmacovigilance
- Compliance Management with 360 ⁰ Reporting
The Conference topics include:
- Global DMS
- Electronic signature
- PIM change
- Submission management
- Linking of regulatory systems
- Long term archiving
In the area of (e)Document management, the conference will focus on:
- Will you meet the requirements of the new ISO standard IDMP on time?
- Listen to case studies of linking regulatory systems
- Get strategies for long-term archiving and ensuring long-term stability data format
- Find out about the implementation of an enterprise-wide DMS as a road to information management
- Use electronic signatures in accordance with the requirements of 21 CFR Part 11
