Application Notes & Whitepapers 2018
Posted: 19 December 2018 | European Pharmaceutical Review | No comments yet
Keeping up with the latest developments in pharma.
Welcome to the Application Notes and Whitepaper supplement of European Pharmaceutical Review, December 2018.
This year’s topics range from API development, cleanroom contamination and water purification through to mass spectrometry, Raman spectroscopy and quality and regulatory compliance.
The theme of data runs throughout, with companies advising on how to manage data transitions and data integrity, and the benefits of laboratory information management systems (LIMS) in the industry.
We hope you enjoy the supplement and would like to thank everyone for their contributions. Some of the Application Notes and Whitepapers are abridged here, in which case the full versions are available to download at europeanpharmaceuticalreview.com/whitepaper.
In this edition:
Representative sampling of solids and turbid media in process raman spectroscopy
A high-quality Raman microscope can be recognised by these 5 criteria
Microbiological considerations in cleanroom validation
Characterising antibody-drug conjugates using micro pillar array columns combined with mass spectrometry (μPAC™-MS)
Real time, low flow, pharmaceutical soil cleanability profiling with TOC and conductivity
Big Data in pharmaceuticals – big opportunities or big challenges or both?
Tracking fate and purge of impurities and calculating carryover
Transforming your bioanalysis operations
Are you facing a complexity crisis?
Quality manufacturing solution – interfacing with third-party systems
The importance of data integrity in current regulation
Biologic drug identification at fill and finish
Verification of three different Opadry whites using a handheld Raman analyser
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