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Understanding the EU In Vitro Diagnostic Regulation (IVDR) and its impact
Discover essential insights into the EU IVDR and its impact on compliance, safety and market access with our comprehensive white paper.
DownloadEverything You Need to Know about Microbiological Challenge Testing
In this whitepaper, we will share some best practices for when to perform a challenge study, how to design and conduct your studies and how to interpret results to help prove food products are stable and safe.
DownloadNavigating Drug Development: Streamlining Efficiency with SGS PACE
Early phase clinical trials - Maxim #3
DownloadManaging Time and Risk
Early phase clinical trials - Maxim #4
DownloadRecruiting the Studied Population in a Timely Manner
Early phase clinical trials - Maxim #5
DownloadExploring the CSDDD
Delve into the EU’s Corporate Sustainability Due Diligence Directive (CSDDD), including its challenges, benefits and how we can help. Download our white paper.
DownloadInnovation Powers Research and Development
Early Phase Clinical Trials - Maxim #6
DownloadSGS PACE
Streamline your drug development pathway from preclinic to FIH/POC.
DownloadThe Basics of Drug-drug Interaction Studies
Gain comprehensive insights into drug-drug interaction (DDI) studies within a clinical development program.
DownloadComparing ISO/IEC 27001:2022 to ISO/IEC 27001:2013. What are the changes?
Discover the key changes between ISO/IEC 27001:2022 and ISO/IEC 27001:2013 – download our white paper now.
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