Dr. Faezeh Eskandari completed a two-day course in Prague, Czech Republic from April 20-21, 2015 on document management and GMP requirements. The course covered topics such as pharmaceutical documentation, electronic document management systems, EU GMP Chapter 4 document types, archiving paper and electronic records, managing multilingual documents, digital signatures, raw data definitions, XML-based document management, and periodic reviews. Workshops were also included on archiving and periodic reviews.

1. Dr. Faezeh Eskandari
has completed a two day ECA-Course on 20 to 21 April 2015 in Praha,
Czech Republic covering the following subject
ECA - Document Management
GMP Requirements and Best Practice
Contents of the course:
An Introduction to Pharmaceutical Documentation
Efficient Usage of electronic Documentation Management Systems (example
Documentum®)
Presentation and Discussion of EU GMP Chapter 4 Document Types
Workshop: Archiving
The Management and Storage of Records (paper vs. electronic records)
Management and Control of multilingual Documents
Digital Signatures
Definition of Raw Data: what you need to know
XML–based Document Management
Workshop: Periodic Review
Heidelberg, 21 April 2015