news
CDMO outsourcing market to reach $36.51bn by 2023
The global pharma contract development and manufacturing organisation (CDMO) outsourcing market is predicted to grow.
List view / Grid view
Lab Equipment
video
On-demand webinar: Increasing Productivity by Leveraging Single Use Technology
The impact of new and alternative monitoring technologies on labor costs in the laboratory and in manufacturing can be significant.
video
On-demand webinar: Leveraging Data Management for Root Cause Identification in Critical Environments
With the increasing employment of sophisticated Data Management software, the collection and evaluation of multiple data has never been easier! However, managing such a large amount of information may represent a challenge, resulting in a potential obstacle to effective identification of the root cause of the environmental OOS associated deviation…
video
On-demand webinar: Complying with USP 729, 788-1788 Regulatory Requirements
Release of parental drugs for injection requires test apparatus to be accurate, precise, reliable and compliant with the latest international regulation.
whitepaper
Application note: New Peak Detection Using the SCIEX OS Software 1.5 MAM Workflow
Liquid chromatography mass spectrometry (LC-MS) is a highly accurate and sensitive platform used in biopharmaceutical research and development.
whitepaper
Scientific poster: Common Laboratory Techniques in the Drug Discovery Workflow
The characterization of novel therapeutics involves many chemical processes.
whitepaper
Whitepaper: Choosing a LIMS or SAP for your laboratory
Would a LIMS or SAP better meet the needs of your company? That is the eternal debate for organizations who are thinking about upgrading their laboratory tracking software to a professional management system - analogous to the Mac vs PC conundrum on an industrial scale.
article
Safeguard patients’ safety with extractables and leachables studies
SGS Life Sciences offers tailored study design and testing for extractables and leachables (E&L) in finished pharmaceutical packaging, process equipment and medical devices, and leachables in final product for clients using single-use systems (SUS).
whitepaper
Whitepaper: Use of accelerated conditions in extractables and/or leachables studies
The purpose of this Position Paper is to consider the scientific basis for accelerating extractables and/or leachables studies via the proper combination of contact temperature and duration (time). Considering this scientific basis, recommendations concerning proper acceleration strategies are provided.
video
Video: µPAC™ Performance at Capillary Flow Rates – PharmaFluidics’ µPAC™ Family
Discover the new µPAC™ C18 capLC column (1 – 15 µl/min) with unrivalled separation power and plug and play connectivity.
whitepaper
Whitepaper: Manage Your Risk: Monitoring the Environment of Aseptic Processes
Risk assessment consists of the identification of hazards and the analysis and evaluation of risks associated with exposure to those hazards.
whitepaper
Case study: Merck Leverages Data and Analytics to Support New Continuous Drug Manufacturing Processes
Over the past couple of years, the European Medicines Agency and US Food and Drug Administration have given approvals to a handful of pharmaceutical companies to manufacture drug products using continuous manufacturing processes.
whitepaper
Scientific poster: Chromatography essentials for performing perfect separations
This free poster compiles all basic chromatography principles needed to develop and run flash and prep HPLC methods.
news
Immunotherapy specialist benefits from Quantum bioprocessing pump
Quantum pump specified for critical UF/DF processes; user says “no other pump could meet all of our needs".
whitepaper
Application note: Rapid Analysis of Genotoxic Nitrosamines by HPLC-MS/MS
Genotoxic impurities (GTI’s) are intermediate, reactive products or degradants formed during drug synthesis, formulation or storage.
