"Do you have all important environmental conditions in view at all times?"
Testo Pharma Solutions
If pharmaceuticals are produced and stored under the wrong climatic conditions, the stability and therefore the efficacy of the drugs can suffer as a result.
Testo can support you in a GMP-regulated environment with:
- Best-in-class data monitoring system
- All-in-one solutions hardware / software / services
- 100% audit-safe
"We guarantee a 100% audit approved data monitoring system!"
In environments where precision is non-negotiable, effective monitoring of temperature and other parameters is essential to guarantee product safety, regulatory compliance, and operational efficiency.
WHY ATTEND:
- Understand the latest trends and regulatory requirements impacting environmental monitoring in biotech
- Discover how automated monitoring systems can improve product quality and safety
- Learn solutions to common temperature monitoring issues affecting operational efficiency
- Explore real-world case studies highlighting successful technology applications
📅 𝐃𝐚𝐭𝐞: July 8, 2025
🕘 𝐓𝐢𝐦𝐞: 9:00 AM & 4:00 PM CET (choose your preferred session)
Best in class software
The testo Saveris software enables comprehensive analysis and evaluation of all recorded measurement parameters - with access from anywhere:
- Detailed logging functions and secure archiving of measurement data
- Audit-proof central data management platform
- Meets requirements of the FDA regarding 21 CFR Part 11 and Annex 11 of the EU GMP Directive.
Broad portfolio of hardware
Our precise and reliable sensor technology forms the basis of our measurement solutions. We rely on state-of-the-art technologies and strict quality controls to ensure that our sensors deliver accurate measurement results:
- Digital probes
- Different communication technologies ( wifi - ethernet - ultrarange)
- Triple storage of data
Our extensive offering of services
Our specially GxP-trained service team accompanies you through all process steps in a customer-oriented and systematic way:
- Temperature mappings
- System qualification
- Software validation
- Maintenance
- Calibration (ISO17025 & ISO9001)
Our applications
Through our collaboration with pharmaceutical companies, we've had the privilege of contributing to projects in these fields:
- Hospitals
- Pharma logistics
- R&D
- Laboratories
- Cleanrooms
- Blood banks
- Biotech
Some references
Continuous monitoring
Immediate detection of deviations
Seamless integration
Avoidance of monitoring gaps
Redundancy and reliability
High data integrity
Compliance with regulations
Avoidance of quality losses
Optimization of processes
"Top 10 requirements to consider when designing your temperature monitoring system"
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Everything in view at all times:
Environmental monitoring with testo Saveris 1
Continuous monitoring and documentation of environmental parameters such as temperature, humidity or differential pressure can quickly become a challenge.
The industry-leading monitoring solution testo Saveris 1 provides automated and efficient support in complying with your regulatory requirements.
Let's meet at SIS Healthcare
Join us on 11-12-13 February 2025 at Sciencepark in Antwerp
In 3 days, you'll explore innovations in ATMP, tackle supply chain challenges, and learn about cutting-edge technologies transforming industries. Engage with experts through keynotes, panels, and networking, and connect with healthcare professionals and students during relaxed site visits and an after-work gathering with food, music, and collaboration.
5 Steps in getting ISO15189 certification
ISO 15189 is an international standard that specifies the requirements for quality and competence in medical laboratories. It ensures that laboratories provide accurate and reliable test results, which are critical for patient care. One of the key areas covered by this standard is temperature monitoring, which is vital for maintaining the integrity of medical samples and reagents
Our Projects
“At Livlina we strongly believe in a high-tech approach” says Karel Van Besien, Director of Quality at Livlina. “For example, our largest warehouse in Sint-Niklaas is 20 years old, but because it was so progressive at the time, it still feels very modern today. When we started looking for a way to check the temperature for our new distribution center in Tessenderlo, we wanted an accurate and fully automated system with extensive data logging. In the pharmaceutical sector, traceability is particularly important, sometimes literally of vital importance, and if there is no data on, for example, the temperature during the entire chain, products may have to be destroyed. That could mean a financial hangover.”
Karel Van Besien
Director of Quality at Livlina
360° GxP services
The testo Saveris data monitoring system enables users to save time and money with automated measurement data management. Other benefits include centralised documentation and a range of different alarm options. The system guarantees the reliable detection, storage and archival of measurement data in production processes, when storing and transporting pharmaceutical products and in clean room air conditioning.
Testo offers full services for qualification/validation. The “Premium” package offers you fully comprehensive GAMP 5 validation, which can include your specific requirements for implementing risk analysis, after which you can skip directly to productive use. The modular and detailed risk analysis process and coherent validation documentation facilitates not only traceability but also the evaluation of future system alterations, quickly and securely.
Finally we offer also on-site services for mapping & calibration (ISO 9001 & ISO 1702). Our engineers and technicians calibrate your measuring systems following your specific requirements. In this way, you may be sure that all calibrations and documentations are performed according to the standards reproducible and traceable.
"In the pharmaceutical industry, unwavering commitment to instrument calibration is vital, as it ensures data integrity and product safety, highlighting the essential role of precision in protecting public health."
Marc Vandenbergh
Head of Calibration Laboratory Testo
"Ensuring product quality in pharmaceutical logistics"
In this Webinar you explore GxP standards and the critical role of environmental monitoring in maintaining product integrity. Discover practical strategies for ensuring medicine safety and hear firsthand from logistics leader Simon Hegele.
Gain insights into best practices for pharmaceutical supply chain management, including vaccine storage. Aimed at industry professionals, this webinar offers valuable guidance for enhancing product quality and patient safety
"What if you could choose between different communication technologies in the same monitoring system?"
Your key benefits
- Real-time monitoring: Keep an eye on all quality-related environmental parameters at all times.
- Efficient documentation: Time and resource-saving recording and documentation of measured values.
- Intelligent alarm system: Use advanced alarm features to anticipate and prevent critical events.
"Always one step ahead"
A guide to early problem detection and securing the working environment in environmental monitoring.
Well-implemented alarm & escalation management is crucial for operational efficiency and quality assurance in environments with critical temperature and humidity requirements.
From complex to easy:
FDA 21 CFR Part 11 in temperature monitoring
21 CFR Part 11 is a regulation set by the U.S. Food and Drug Administration (FDA) that establishes criteria for the use of electronic records and electronic signatures (ERES) in the pharmaceutical, biotechnology, and other industries regulated by FDA. This part of the Code of Federal Regulations ensures that electronic records and signatures have the same level of trustworthiness and reliability as traditional paper records and handwritten signatures.
5 stories – 1 solution: How testo Saveris 1 convinces in use
When it comes to environmental monitoring, companies are constantly faced with complex challenges: inadequate WLAN coverage, limitations in the technical equipment available to teams, the need for seamless calibration and integration of different measurement systems, and the need for customized consulting services. These scenarios require well thought-out solutions.
How can we at Testo meet these diverse requirements without us or our customers having to compromise on quality and safety? Here, five success stories show how testo Saveris 1 overcomes these challenges and improves efficiency and reliability in different environments.
What to do if there is insufficient WLAN coverage ?
How can employees be alerted about limit violations without SMS and e-mail ?
How to avoid measurement gaps during calibration ?
Is it possible to display measured values from different sources on one dashboard ?
Which support services can Testo offer companies in the field of environmental monitoring ?
Connect with your LIMS
REST-API: Interface for Testo Saveris 1
Centralize your monitoring
Display all parameters on a unified dashboard
Connect with you LIMS
"Revolutionize patient care and enhance clinical trial efficiency with our cutting-edge temperature monitoring solutions, ensuring precision, compliance, and real-time data insights tailored for the pharmaceutical industry."
Stefan Van Vooren
Testo Pharma Solutions