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& insights
We’ve spent the past 30 years working with some of the world’s leading pharma companies to help them deliver drugs safely to patients, which gives us the data and perspective to offer unique insights into temperature monitoring and the topics that shape them. Here you’ll find our take on some of them.
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Achieving FDA and EMA Compliance in Temperature Monitoring
Many pharmaceuticals and biological products require specific temperature conditions during manufacturing, storage, and transport to ensure their quality and safety. Failure to maintain these conditions can lead to product degradation, making them less effective or even dangerous. To protect public health, regulatory authorities like the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have established strict guidelines to manage these products. To comply with these regulations, life science companies must adopt advanced temperature monitoring systems that can track and record conditions continuously and reliably. This whitepaper explains the main requirements from both the FDA and EMA, the role of technology in maintaining compliance, and the best practices for setting up effective temperature monitoring systems.
Read moreDownload Whitepaper
Proactive Temperature Management: The Key to a More Resilient Pharma Supply Chain
At this year's LogiPharma Europe 2025 in Lyon, Anita Leposa, Key Account Manager at TSS, and Neil Malkin, Business Process Owner for Temperature Management at AstraZeneca, took the stage to discuss one of the most pressing challenges in the pharmaceutical supply chain: temperature excursions and their impact on medicine availability.
Read moreDownload Whitepaper
Join Us at LogiPharma Europe 2025
Reactive Excursion Intervention with Real-Time Temperature Data: From reactive crisis management to proactive supply chain optimization
Read moreDownload Whitepaper
TSS Receives CDP SME Climate Score 'SME B' for Strong Climate Actions
TSS, a global company specializing in temperature monitoring for the pharmaceutical supply chain, is proud to announce that it has received an 'SME B' rating from the 2024 CDP SME Climate Score. This recognition highlights TSS’s commitment to being open about its environmental impact and taking steps to reduce it.
Read moreDownload Whitepaper
Future-Proofing Clinical Trials: How Sponsors Can Up-Scale Through Automation
At this year’s Clinical Trial Supply Europe event in Barcelona, TSS took center stage to discuss one of the most pressing challenges in clinical trial supply chains—temperature monitoring. Our Key Account Manager, Anita Leposa, highlighted how automation is revolutionizing temperature integrity management, reducing manual work, and ensuring compliance for global pharmaceutical sponsors.
Read moreDownload Whitepaper
Celebrating Women in Tech
February 11 marks the International Day of Women and Girls in Science, a day dedicated to recognizing the invaluable contributions of women in STEM fields and inspiring future generations to follow in their footsteps.
Read moreDownload WhitepaperShowing news
Proactive Temperature Management: The Key to a More Resilient Pharma Supply Chain
At this year's LogiPharma Europe 2025 in Lyon, Anita Leposa, Key Account Manager at TSS, and Neil Malkin, Business Process Owner for Temperature Management at AstraZeneca, took the stage to discuss one of the most pressing challenges in the pharmaceutical supply chain: temperature excursions and their impact on medicine availability.
Read moreDownload WhitepaperJoin Us at LogiPharma Europe 2025
Reactive Excursion Intervention with Real-Time Temperature Data: From reactive crisis management to proactive supply chain optimization
Read moreDownload WhitepaperTSS Receives CDP SME Climate Score 'SME B' for Strong Climate Actions
TSS, a global company specializing in temperature monitoring for the pharmaceutical supply chain, is proud to announce that it has received an 'SME B' rating from the 2024 CDP SME Climate Score. This recognition highlights TSS’s commitment to being open about its environmental impact and taking steps to reduce it.
Read moreDownload WhitepaperFuture-Proofing Clinical Trials: How Sponsors Can Up-Scale Through Automation
At this year’s Clinical Trial Supply Europe event in Barcelona, TSS took center stage to discuss one of the most pressing challenges in clinical trial supply chains—temperature monitoring. Our Key Account Manager, Anita Leposa, highlighted how automation is revolutionizing temperature integrity management, reducing manual work, and ensuring compliance for global pharmaceutical sponsors.
Read moreDownload WhitepaperCelebrating Women in Tech
February 11 marks the International Day of Women and Girls in Science, a day dedicated to recognizing the invaluable contributions of women in STEM fields and inspiring future generations to follow in their footsteps.
Read moreDownload Whitepaper
Clinical Trial Supply Europe Event 2025
Curious about how to up-scale you Clinical Trials? Join us at the 26th Annual Clinical Trial Supply Europe in Barcelona to explore your possibilities for optimizing the supply chain.
Read moreDownload WhitepaperShowing Supply chain articles
Achieving FDA and EMA Compliance in Temperature Monitoring
Many pharmaceuticals and biological products require specific temperature conditions during manufacturing, storage, and transport to ensure their quality and safety. Failure to maintain these conditions can lead to product degradation, making them less effective or even dangerous. To protect public health, regulatory authorities like the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have established strict guidelines to manage these products. To comply with these regulations, life science companies must adopt advanced temperature monitoring systems that can track and record conditions continuously and reliably. This whitepaper explains the main requirements from both the FDA and EMA, the role of technology in maintaining compliance, and the best practices for setting up effective temperature monitoring systems.
Read moreDownload WhitepaperJoin Us at LogiPharma Europe 2025
Reactive Excursion Intervention with Real-Time Temperature Data: From reactive crisis management to proactive supply chain optimization
Read moreDownload WhitepaperFuture-Proofing Clinical Trials: How Sponsors Can Up-Scale Through Automation
At this year’s Clinical Trial Supply Europe event in Barcelona, TSS took center stage to discuss one of the most pressing challenges in clinical trial supply chains—temperature monitoring. Our Key Account Manager, Anita Leposa, highlighted how automation is revolutionizing temperature integrity management, reducing manual work, and ensuring compliance for global pharmaceutical sponsors.
Read moreDownload Whitepaper
Sustainable Temperature Management: A Key to Greener Clinical Trials
As the global healthcare industry focuses more on sustainability, temperature management in clinical trials is becoming more important. Research organizations and clinical trial sponsors are starting to see that making clinical trial processes more sustainable is not only good for the environment but also improves efficiency and cuts costs.
Read moreDownload Whitepaper
10 Common Mistakes to Avoid During Customer Onboarding
Customer onboarding is one of the most important steps in making sure your customers are happy and confident in using your product. At TSS, we help companies in life sciences monitor complex temperature budgets with our advanced automated cloud software and temperature loggers. Making the onboarding process smooth is key to long-term customer satisfaction.
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TSS Keeps EcoVadis Silver Medal Despite Tougher Standards in 2024
TSS, a leading provider of temperature-monitoring solutions for the life-science industry, proudly announces that it has retained the EcoVadis Silver Medal for the second consecutive year. This recognition is a testament to TSS’s ongoing commitment to sustainability, even as EcoVadis raised the bar for its assessment criteria in 2024.
Read moreDownload WhitepaperShowing clinical articles
Achieving FDA and EMA Compliance in Temperature Monitoring
Many pharmaceuticals and biological products require specific temperature conditions during manufacturing, storage, and transport to ensure their quality and safety. Failure to maintain these conditions can lead to product degradation, making them less effective or even dangerous. To protect public health, regulatory authorities like the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have established strict guidelines to manage these products. To comply with these regulations, life science companies must adopt advanced temperature monitoring systems that can track and record conditions continuously and reliably. This whitepaper explains the main requirements from both the FDA and EMA, the role of technology in maintaining compliance, and the best practices for setting up effective temperature monitoring systems.
Read moreDownload WhitepaperFuture-Proofing Clinical Trials: How Sponsors Can Up-Scale Through Automation
At this year’s Clinical Trial Supply Europe event in Barcelona, TSS took center stage to discuss one of the most pressing challenges in clinical trial supply chains—temperature monitoring. Our Key Account Manager, Anita Leposa, highlighted how automation is revolutionizing temperature integrity management, reducing manual work, and ensuring compliance for global pharmaceutical sponsors.
Read moreDownload WhitepaperClinical Trial Supply Europe Event 2025
Curious about how to up-scale you Clinical Trials? Join us at the 26th Annual Clinical Trial Supply Europe in Barcelona to explore your possibilities for optimizing the supply chain.
Read moreDownload WhitepaperSustainable Temperature Management: A Key to Greener Clinical Trials
As the global healthcare industry focuses more on sustainability, temperature management in clinical trials is becoming more important. Research organizations and clinical trial sponsors are starting to see that making clinical trial processes more sustainable is not only good for the environment but also improves efficiency and cuts costs.
Read moreDownload Whitepaper
How to Scale Up Your Clinical Trials
Pharmaceutical companies are under pressure to bring new drugs to market quickly. This urgency is driven by the needs of patients, requirements from authorities, and investors. Clinical trials are a crucial part of this process, but they can be delayed by manual processes.
Read moreDownload Whitepaper
Enhancing Product Quality and Compliance at Clinical Sites
In the pharmaceutical industry, maintaining precise temperature control is paramount to ensuring product quality and compliance with regulatory standards. The integrity of pharmaceutical products is heavily reliant on storage conditions, with deviations in temperature potentially compromising their efficacy and safety.
Read moreDownload WhitepaperShowing all technology articles
10 Steps to Navigating Sustainability in the Pharma Supply Chain
In the complex world of pharmaceuticals, sustainability is becoming a key part of business strategy. The push for a greener future is driven not only by government rules but also by the expectations of communities and customers. However, making the supply chain sustainable while balancing costs and maintaining high quality can be challenging. This requires careful planning and a commitment to long-term goals.
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Balancing Cost and Quality in the Pharmaceutical Supply Chain: A Quick Guide
In the life-science industry, finding the right balance between cost and quality in the supply chain is crucial. This balance ensures that pharma companies remain financially healthy while delivering safe and effective products to patients. However, achieving this balance can be challenging due to the complexities of quality management, procurement, and temperature control.
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TSS Celebrates WTISD 2024: Embracing Innovation, Digitalisation, and Sustainability
World Telecommunication & Information Society Day (WTISD), celebrated annually on May 17th, highlights the pivotal role of digital technologies in fostering societal progress. This day serves as a reminder of the transformative power of innovation and digitalisation in building a sustainable future. At TSS, we are dedicated to leveraging advanced technologies to enhance the pharmaceutical supply chain while promoting sustainability.
Read moreDownload WhitepaperEnhancing Product Quality and Compliance at Clinical Sites
In the pharmaceutical industry, maintaining precise temperature control is paramount to ensuring product quality and compliance with regulatory standards. The integrity of pharmaceutical products is heavily reliant on storage conditions, with deviations in temperature potentially compromising their efficacy and safety.
Read moreDownload Whitepaper
TSS Achieves Coveted ISO/IEC 17025 Calibration Accreditation
TSS AB proudly announces its Calibration Laboratory's ground-breaking achievement of ISO/IEC 17025 accreditation by Swedac. This milestone sets a new standard for precision and reliability in temperature monitoring services.
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TSS Welcomes Thomas Lindén as New Chief Technology Officer
TSS, a leading temperature monitoring solutions provider, is pleased to announce the appointment of Thomas Lindén as its new Chief Technology Officer (CTO). In this role, Thomas Lindén will play a crucial part in shaping the company's technological landscape and driving its growth strategies.
Read moreDownload WhitepaperShowing all events
Proactive Temperature Management: The Key to a More Resilient Pharma Supply Chain
At this year's LogiPharma Europe 2025 in Lyon, Anita Leposa, Key Account Manager at TSS, and Neil Malkin, Business Process Owner for Temperature Management at AstraZeneca, took the stage to discuss one of the most pressing challenges in the pharmaceutical supply chain: temperature excursions and their impact on medicine availability.
Read moreDownload WhitepaperJoin Us at LogiPharma Europe 2025
Reactive Excursion Intervention with Real-Time Temperature Data: From reactive crisis management to proactive supply chain optimization
Read moreDownload WhitepaperClinical Trial Supply Europe Event 2025
Curious about how to up-scale you Clinical Trials? Join us at the 26th Annual Clinical Trial Supply Europe in Barcelona to explore your possibilities for optimizing the supply chain.
Read moreDownload Whitepaper
LogiPharma Lyon 2024
The Future of Temperature Monitoring: How to lower the CO2 footprint with a Circular Supply Solution
Read moreDownload Whitepaper
Join us at Clinical Trial Supply Europe 2024 in Barcelona
Are you in pursuit of optimizing the temperature management of your clinical trials supply chain? Get inspired by experts from the field, and learn from their experiences.
Read moreDownload Whitepaper
NECSO Cambridge 2023
Where do the majority of your temperature excursions occur? Why not eliminate them?
Read moreDownload WhitepaperShowing all whitepapers
Achieving FDA and EMA Compliance in Temperature Monitoring
Many pharmaceuticals and biological products require specific temperature conditions during manufacturing, storage, and transport to ensure their quality and safety. Failure to maintain these conditions can lead to product degradation, making them less effective or even dangerous. To protect public health, regulatory authorities like the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have established strict guidelines to manage these products. To comply with these regulations, life science companies must adopt advanced temperature monitoring systems that can track and record conditions continuously and reliably. This whitepaper explains the main requirements from both the FDA and EMA, the role of technology in maintaining compliance, and the best practices for setting up effective temperature monitoring systems.
Read moreDownload Whitepaper
White paper: the future, today - the next generation of temperature monitoring
New technologies for tracking and temperature logging hold great potential, but which to choose? Get a copy of our latest white paper.
Read moreDownload Whitepaper
White paper: The next step to automating clinical trials
Temperature management is critical when it comes to ensuring patient safety in clinical development, but we continue to use legacy point solutions that require heavy manual processes and duplication of data.
Read moreDownload Whitepaper