White Papers
Our white papers and technical bulletins are written by industry experts from many different fields, exploring and commentating on a range of complex subjects.
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Developing Effective Risk Mitigation Practices in Response to California Proposition 65
Businesses operating in California, USA, need to understand Proposition 65 (Prop 65). In this white paper we explain Prop 65 and consider effective risk mitigation practices. |
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Identification of Surface Impurities and Particles by Means of Special Analysis Methods
This paper describes some special analytical techniques, their advantages and disadvantages and their application for particle material identification as well as for surface contamination characterization. |
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Determining the Structure of Impurities
In the pharmaceutical industry, impurities can arise at numerous points in the various processes used. They could occur during research and development, but also during production of the active substances. |
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Academic Collaboration with Contract Research Organizations: Reaching Out to the Right Expertise at the Right Time
Drug development is a lengthy and winding road with many obstacles and challenges to be overcome. |
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European Union ROHS2 - Understanding Requirements and Compliance Strategies
The EU’s RoHS2 Directive restricts the use of certain hazardous substances in electrical and electronic equipment. In this white paper we consider the terms of this regulation and the ways stakeholders can ensure compliance. |
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Global Access Program (GAP) for Electrical & Electronics (E&E) Products
This white paper summarizes how to demonstrate compliance with and achieve certification against the relevant national and international standards for EE products. |
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End to End SDTM Automation: A Metadata Centric Approach
The implementation of a metadata repository (MDR) is the first step toward a metadata driven approach; we at SGS went a few steps furhter and built in-house tools that are linked to the MDR to achieve end-to-end automation of the SDTM workflow. |
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Extractables & Leachables in Single-Use Systems
Biopharmaceutical Safety: Identifying and Quantifying Extractables and Leachables from Single-Use Plastic Bioprocess Bags |
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Understanding the Forest Product Chain-of-Custody Certification Standard
A discussion about the challenges, impacts and opportunities associated with Forest Product Chain of Custody (CoC). |
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How Can You Improve Product Safety? Enhance Your Quality Management System With ISO 9001:2015
This discusses the core requirements of the new ISO 9001:2015 Quality Management System standard and its benefits to organizations. |