Qualification with Data Integrity in the Pharmaceutical Sector

This seminar is designed to strengthen your understanding of qualification processes within the pharmaceutical sector and to enhance the long-term organization, traceability, and data-integrity compliance of Anton Paar documentation through the use of AP Connect.

In the morning session, you will explore the theoretical foundations, including pharmaceutical documentation requirements, the functionalities of AP Connect, and the concept of tolerances. The afternoon session focuses on hands-on practice, giving you the opportunity to work directly with AP Connect and apply what you have learned by performing practical exercises related to tolerances.

• Understanding qualification documents: Learn how to interpret and apply Anton Paar’s qualification documents, including their structure, purpose, and role in a GMP-regulated environment.
• Understanding tolerances and measurement uncertainty: Gain clarity on how tolerances are defined, how to interpret them, and how measurement uncertainty influences result evaluation.
• Managing and evaluating data through AP Connect: Learn how AP Connect captures, organizes, and evaluates measurement data to support data integrity, traceability, and efficient documentation workflows.

目標群組: Pharma Specialists, Lab Manager, QA Professionals or IT System Owner
必要條件: Basic knowledge of GMP is required

地點: Baden, Schweiz, Anton Paar Switzerland AG Brown Boveri Strasse 12, 5400 Baden
主辦方: Mirko Rüggeberg
費用: CHF 750
註冊截止時間: 2026年4月28日

聯絡人和註冊承辦人:
Selina Zemp
電話: +41 62 544 18 25
selina.zemp[at]anton-paar.com