Join our webinar on the latest cold storage technology for the pharmaceutical industry. Discover how forced-air convection can revolutionize your operations, optimize workflow, and protect sample integrity. Register now to stay ahead in pharmaceutical manufacturing.
Join us for an insightful webinar focused on streamlining processes and leveraging digital solutions to automate temperature compliance. If you and your team find yourselves spending excessive time on manual tasks and making avoidable mistakes, this webinar is designed specifically for you!
Going from data to action – are you making the most of your temperature mapping reports? Join us in a dive into how to get the most out of the data from your mappings.
Are you worried about temperature monitoring audits? Join us for a talk where we will share best practices and practical steps to help you efficiently prepare for temperature compliance audits, avoiding frustrations and uncertainties. Don’t wait until the last minute to start your preparation – be proactive and navigate the audit process with confidence.
Join us to learn the different elements you should take into account 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.
This webinar discusses the importance of creating a robust temperature mapping protocol for a successful mapping exercise. Validation experts will provide insights into developing a protocol suitable for specific needs, covering the essential elements, what not to include, and common errors and lackings of protocols.
Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.
This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.
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