Insight into the current specifications on the topics: Software Validation & Data Integrity
New to the pharmaceutical world and not yet familiar with all the regulations?
Are you new to the pharmaceutical world and looking for support in taking your first steps in this exciting and complex world?
In this webinar you will learn more about the requirements of the EU GMP Annex 11- Computerised System. We will give you insights for the practical implementation for your daily work. We cordially invite you to our free webinars, where we will answer all questions relevant to you as an expert.
Content:
- Brief overview of Annex 11 - Computerised Systems
- Explanation of the current requirements on the subject of data integrity
- Assistance with software validation
Target:
-
Employees from pharmaceutical companies who would like to gain initial access to the topic of software validation.
-
People generally interested in the practical application and implementation of GMP requirements
-
Distributors who would like to advise customers from the pharmaceutical industry specifically on the subject of software validation
Duration: 1,5 hour
Webinar - Speaker:
Sebastian Schwarz - Market Manager Pharma
Degree as chemical and biological engineer in Erlangen, Germany
- 7 years experience as a consultant in a GMP controlled environment
- Projects in the areas of calibration, qualification and validation for pharmaceutical manufacturers throughout Europe
Phone: +49 841-9547837 E-Mail: Sebastian.Schwarz@ Xylem.com