
-
00
days
-
00
hours
-
00
minutes
-
00
seconds
Date
- Jul 08 2025
Two sessions available to choose from:
9:00 AM – 10:30 AM
Central European Time
AND
4:00 PM – 5:30 PM
Central European Time
Overview
Join us for an expert-led session exploring one of the most pressing issues in the Biotech industry: how to effectively monitor temperature and other environmental parameters in highly regulated and quality-sensitive environments.
In this knowledge-focused webinar, you’ll gain valuable insights into the specific challenges that Biotech companies face in monitoring environmental conditions, especially temperature. While the first part of the session offers an overview of industry challenges and regulatory requirements, the core focus will be on practical strategies and system solutions to meet these challenges head-on.
Have you ever wondered…
How to centralize temperature control of all ultra-freezers, temperature-controlled rooms, and storage?
How to guarantee the sterilization temperature inside the autoclave?
How to improve cell growth with efficient temperature monitoring in the incubator?
Learn the answers to these questions and much more in our webinar!
Learning Objectives:
By the end of this webinar, you will:
- Understand the latest trends and regulations impacting environmental monitoring in the biotech sector.
- Learn how automated environmental monitoring systems can enhance product quality and safety.
- Learn how to solve common challenges in temperature monitoring that decrease operational efficiency.
- Explore case studies demonstrating successful applications of these technologies.
Benefits of Attending:
In the biotech industry, precise environmental monitoring is not an option. It’s a regulatory, operational, and scientific necessity. This webinar dives into the real-world challenges biotech companies face when monitoring critical parameters across incubators, sterilizers, cleanrooms, stability chambers, and more. Additionally, you will learn how monitoring systems help you comply with regulations – such as 21 CFR Part 11 – while guaranteeing product quality and safety.
Instructor Credentials:
• Youssef Khattabi, has over 10 years of experience in the pharma and tech industries. As a Subject Matter Expert Pharma at Testo, he focuses on environmental monitoring solutions, ensuring compliance and efficiency for pharmaceutical clients. His expertise spans LIMS, GAMP, GxP and solution selling.
• Dr. Fábio A. S. Leite, is a Subject Matter Expert for the Pharma sector at Testo, committed to advancing innovative environmental monitoring solutions and improving monitoring practices and data integrity. He holds a doctorate degree in Natural Sciences and has over five years of experience in the development of temperature indicators and smart labels, as well as a deep knowledge of data science.
Don’t miss out on this opportunity to learn how to optimize your environmental monitoring at this must-attend webinar.
Speakers
-
Youssef KhattabiSubject Matter Expert Pharma
With a master’s in business & Strategy and a bachelor’s in computer and information sciences, Youssef has over 10 years of experience in the pharma and tech industries. As a Subject Matter Expert Pharma at Testo, he focuses on environmental monitoring solutions, ensuring compliance and efficiency for pharmaceutical clients. His expertise spans LIMS, GAMP, GxP and solution selling.
-
Dr. Fábio A. S. LeiteSubject Matter Expert Pharma
Dr. Fábio A. S. Leite is a Subject Matter Expert for the Pharma sector at Testo, committed to advancing innovative environmental monitoring solutions and improving monitoring practices and data integrity. He holds a doctorate degree in Natural Sciences and has over five years of experience in the development of temperature indicators and smart labels, as well as a deep knowledge of data science.
Partner

Testo Saveris GmbH
Website
https://www.testo.com/en/solutions/regulatory-monitoring-systemTesto Saveris GmbH develops innovative digital solutions in the Black Forest for automated monitoring and documentation of environmental parameters like temperature, humidity, and pressure. Precise sensors, intelligent software, and robust hardware ensure efficiency, data security, and compliance with regulations such as FDA 21 CFR Part 11 and EU-GMP Annex 11. Customers benefit from a secure platform, proactive quality management, and seamless process integration.
-
Who Should Attend:
Target Group:
Pharma, Biotech; Laboratories, Hospitals; Logistics; Chemical Industries; Cosmetic Industries; Waste managementPositions:
QA managers; IT; Facility Manager; Operation Manager; Auditors; Security Manager; Production Manager; Laboratory Manager; COOs; CTOs - Skill Level: Intermediate
-
Topics:
- Navigating Environmental Monitoring Challenges: Discover the latest challenges faced in Biotech regarding monitoring environmental parameters and how to address them effectively.
- Ensuring Regulatory Compliance: Learn about vital regulations that surround the Biotech sector and how to address them to guarantee proper compliance.
- Harnessing System Integration for Efficiency: Dive into critical points where environmental monitoring is critical in the Biotech sector and how monitoring systems can help support your operations guaranteeing maximum product quality and safety.
-
Special event information:
All participants will get a complimentary certificate of attendance courtesy of the webinar's partner - Testo.
Date
- Jul 08 2025
Two sessions available to choose from:
9:00 AM – 10:30 AM
Central European Time
AND
4:00 PM – 5:30 PM
Central European Time
-
00
days
-
00
hours
-
00
minutes
-
00
seconds
Speakers
-
Youssef KhattabiSubject Matter Expert Pharma
With a master’s in business & Strategy and a bachelor’s in computer and information sciences, Youssef has over 10 years of experience in the pharma and tech industries. As a Subject Matter Expert Pharma at Testo, he focuses on environmental monitoring solutions, ensuring compliance and efficiency for pharmaceutical clients. His expertise spans LIMS, GAMP, GxP and solution selling.
-
Dr. Fábio A. S. LeiteSubject Matter Expert Pharma
Dr. Fábio A. S. Leite is a Subject Matter Expert for the Pharma sector at Testo, committed to advancing innovative environmental monitoring solutions and improving monitoring practices and data integrity. He holds a doctorate degree in Natural Sciences and has over five years of experience in the development of temperature indicators and smart labels, as well as a deep knowledge of data science.
Partner

Testo Saveris GmbH
Website
https://www.testo.com/en/solutions/regulatory-monitoring-systemTesto Saveris GmbH develops innovative digital solutions in the Black Forest for automated monitoring and documentation of environmental parameters like temperature, humidity, and pressure. Precise sensors, intelligent software, and robust hardware ensure efficiency, data security, and compliance with regulations such as FDA 21 CFR Part 11 and EU-GMP Annex 11. Customers benefit from a secure platform, proactive quality management, and seamless process integration.