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Qualification with Data Integrity in the Regulated Sectors

Qualification with Data Integrity in the Regulated Sectors

Capacitación avanzada

This seminar is designed to strengthen your understanding of qualification processes within the regulated sectors 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.

Participants are encouraged to submit their specific questions in advance. Our specialists will review these topics and address possible solutions during the seminar.

Georg Roth-Kapori, DI Thomas Kamrat, Mirko Rüggeberg (Idioma: English)

Grupo objetivo: Pharma Specialists, Lab Manager, QA Professionals or IT System Owner
Requisitos previos: Basic knowledge of GMP is required

Lugar: Baden, Schweiz, Anton Paar Switzerland AG Brown Boveri Strasse 12, 5400 Baden
Organizador: Mirko Rüggeberg
Costos: CHF 750
Fin de inscripción: 28 abr 2026

Persona de contacto e inscripción:
Jasmina Gajicic
Tel.: +41 56 544 01 65
jasmina.gajicic[at]Anton-Paar.com

Georg Roth-Kapori

Georg Roth-Kapori is part of the Global Pharma Team at Anton Paar. He holds a master degree in organic chemistry and food development and has more than 20 years of experience in food and pharmaceutical industry standards and regulations. For the past 10 years, he has been responsible for pharmaceutical requirements, instrument qualification documentation, and training at Anton Paar for regulated markets. Furthermore, he is a keynote speaker for Data Integrity, ALCOA++, cGMP, GAMP5 at Concept Heidelberg.

Thomas Kamrat

After graduating in chemistry from the Technical University of Graz, Thomas Kamrat worked as a scientist for several years before moving into industry R&D and quality management. He has been a Product Manager at Anton Paar since 2016 and is responsible for the AP Connect software.

Mirko Rüggeberg

Mirko Rüggeberg has been the Pharma Application Specialist at Anton Paar Switzerland since April 2025. In this role, he acts as a bridge between customer needs and Anton Paar’s solutions, supporting projects from the initial application discussion through to instrument installation and SOP support when required.

With his background as a seasoned service engineer and his experience working in the pharmaceutical industry as a customer, Mirko is well versed in regulated environments. He brings a practical, solution-oriented approach and works closely with customers to find the best possible solution together.