Overcoming Data Logger Calibration Challenges in GxP environments


Aug 31 2023


CEST Berlin
15:00 - 16:30

The event is finished.

Learning Type

Free Live Webinar,
New Date,


Calibrations can be laborious and, in truth, quite a painful process. Whether you work in pharma, biotech, or any other life science industry, you must keep an overview of all calibrations, ensure that each specific logger is calibrated on time, document and store certificates, locate this documentation for audits, and so on.

Deciding on the type of calibration and calibration points can also be difficult if you are not equipped for the task. Furthermore, understanding how the sensor or datalogger measures can impact what and how you measure.

In this webinar, we’ll discuss how to overcome these challenges.

We’ll dive into the different elements you should consider when selecting the type of calibration and choosing calibration points, as well as the uncertainties related to calibration and measurement of environmental parameters in a GxP storage environment.


-How the way sensors or data loggers measure will impact your results
-Which calibration elements should you have ready in case of an audit
-What traceability means and why it’s important
-The difference between an accredited and a traceable calibration
-The uncertainties related to environmental monitoring.


  • Jakob Konradsen
    Jakob Konradsen
    Co-Founder & Chief Quality Officer at Eupry

    Jakob Konradsen has a background in electrical engineering and has worked with quality and validation for his entire work life. Jakob has broad experience within the thermal validation and calibration field, emphasizing temperature validation of everything from temperature-controlled units to large-scale warehouses and transport vehicles. Jakob is passionate about finding solutions that balance regulatory requirements with a cost-effective and pragmatic approach and a risk-based approach.

  • Anja Lundin Jacobsen
    Anja Lundin Jacobsen
    QA/QC Lead

    Anja has a background in biomedical laboratory science and
    has previously worked as a laboratory technician in clinical
    microbiology for more than seven years. She also holds a
    master’s degree in Techno-Anthropology.
    Today, she works as QA/QC Lead at Eupry in charge of the
    daily operations in the company’s ISO17025-accredited
    calibration lab.



Eupry provides a complete suite of solutions to monitor and perform validation of temperature, CO2, humidity, and differential pressure for regulated industries. Eupry runs an accredited ISO/IEC 17025 calibration laboratory. Their innovative and patented products are constantly pushing the industry's limits.

  • Who Should Attend:

    Anyone who deals with system validation and qualification, such as ;
    Head of Quality, QualityAssurance Manager, Quality Control Manager, Lab Manager, Facility Manager (Validation Engineer)

  • Skill Level: Novice, Intermediate , Expert
  • Special event information:

    All participants will get a free certificate of attendance courtesy of our event's sponsor Eupry

What people are saying

Are You Ready To join us?

Share the Event

Thursday May 2
17:00 - 18:30 Taking risks: ICH Q9 (R1) Quality Risk Management
Local Time:
May 02 2024 |
11:00 - 12:30
Thursday May 16
16:00 - 17:30 Unlocking the Power of Root Cause Analysis in Quality Management Systems
Local Time:
May 16 2024 |
10:00 - 11:30
No event found!


Please check your spam folder. If the email landed in spam, make sure to add us as a contact, so it doesn’t happen again. 

If the email is not in the spam folder, please try using a different email address. Sometimes, company security measures intercept email before they get to your mailbox. 

If you get an error when clicking the confirmation link, it has probably something to do with a company internal security measures that change the link.

Please try registering again and opening the email on another device or forwarding the email to your private email.

If everything fails, please register with your private email address. 

If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days. 

Yes, our event partners will email you the event recording within several weeks. 

Leave a Reply


Weekly Industry Insights &
tips for success

Join thousands of pharma professionals on an enlightening journey. 

Subscribe to our weekly newsletter to stay current with the latest industry trends, compliance and skyrocket your career.