Top News

Mar 20, 2018
Sponsored Content
By PPD
Join Gaurav Bhatnagar and Chris Komelasky from PPD to gain insight on how a strategic, data-driven approach to feasibility can help address industry challenges by connecting the most relevant patient, site and investigator data with analytic tools and targeted processes.

Live: Tuesday, 20 March, 2018 | 11 am EDT | 8 am PDT | 1500 GMT | 1600 CET / On Demand available after airing until 20 March, 2019.

Register free: http://www.appliedclinicaltrialsonline.com/act_w/data
Feb 28, 2018
Sponsored Content
The term “FDA audit” can trigger many responses, including dread and panic. It also raises many questions. What triggers a regulatory audit? How has the FDA changed its auditing strategy and what are they focused on? What systems are likely to get inspected? In addition to answering these questions, this webcast will focus on ensuring data integrity in an analytical laboratory. Join us to learn from Humera Khaja, Agilent’s software compliance expert with nearly a decade of regulated software experience.

Live: North America: Wednesday, 28 Feb., 2018 | 11 am EST | 1600 GMT | 2130 IST / On Demand available after airing until 28 Feb., 2019.

Register free: http://www.chromatographyonline.com/lcgc_w/inspection
Feb 12, 2018
The Column
This article outlines a method for the analysis of 21 terpenes in a variety of samples with a sub 9-min elution time.
Jan 31, 2018
Sponsored Content
Want to begin cannabis testing but don’t know where to start? Register now to find out how even somebody with no previous GC experience can start in house testing of cannabis samples.

Live: Wednesday, Jan. 31, 2018 | 1 pm EST | 12 pm CST | 10 am PST / On Demand available after airing until Jan. 31, 2019.

Register free: http://www.chromatographyonline.com/lcgc_w/analysis_cannabis
Jan 25, 2018
Sponsored Content
Live: Thursday, 25 Jan., 2018 | 11 am EST | 10 am CST | 1600 GMT | 1700 CET / On Demand available after airing until Jan., 25, 2019.

Register free: http://www.pharmexec.com/pe_w/revolution
Jan 25, 2018
Sponsored Content
Live: Thursday, 25 Jan., 2018 | 11 am EST | 10 am CST | 1600 GMT | 1700 CET / On Demand available after airing until Jan., 25, 2019.

Register free: http://www.pharmexec.com/pe_w/revolution
Jan 25, 2018
Sponsored Content
This webcast will provide researchers with information about two topics: advancing cell culture profiling using a method package with LC-MS/MS, and utilizing a proprietary sample prep kit for multi-product antibody PK studies by LC-MS/MS. Attendees will learn how these items can help analysis faster, easier, and more effective.

Live: Thursday, Jan., 25, 2018 | 1 pm EST | 12 pm CST | 10 am PST / On Demand available after airing until Jan., 25, 2019.

Register free: http://www.biopharminternational.com/bp_w/analysis
Jan 25, 2018
Sponsored Content
The term “FDA audit” can trigger many responses, including dread and panic. It also raises many questions. What triggers a regulatory audit? How has the FDA changed its auditing strategy and what are they focused on? What systems are likely to get inspected? In addition to answering these questions, this webcast will focus on ensuring data integrity in an analytical laboratory. Join us to learn from Humera Khaja, Agilent’s software compliance expert with nearly a decade of regulated software experience.

Live: North America: Thursday, 25 Jan., 2018 | 9 am EST | 1400 GMT | 1930 IST / On Demand available after airing until 25 Jan., 2019.

Register free: http://www.chromatographyonline.com/lcgc_w/inspection
Jan 24, 2018
Sponsored Content
This interactive webcast will illustrate “what good looks like” and provide an understanding of where your Medical Affairs organization falls in relationship to your peers. Attendees will also walk away with guidance on the three components of the Strategic Medical Platform as a solid foundation on which medical strategies and tactics can subsequently be built.

Live: Wednesday, 24 Jan., 2018 | 11 am EST | 10 am CST | 1600 GMT | 1700 CET / On Demand available after airing until 24 Jan., 2019.

Register free: http://www.pharmexec.com/pe_w/benchmarking
Jan 24, 2018
Sponsored Content
Selected ion flow tube mass spectrometry (SIFT-MS) is a cutting-edge direct MS technique for real-time, quantification of trace volatiles to sub-part-per-billion (ppb) levels, including chromatographically challenging ones such as formaldehyde, formic acid, and ammonia. Join us to learn how this direct analysis technique can be successfully validated in accordance with ICH Q2(R1) Guidelines to achieve GMP-compliant data suitable for regulatory submissions. A case study covering the quantification of formaldehyde in the headspace of a packaged pharmaceutical product illustrates this high-throughput analytical approach.

Live: Europe: Wednesday, 24 Jan., 2018 | 1400 GMT | 1500 CET / North America: Wednesday, January 24, 2018 | 11 am EST | 10 am CST | 8 am PST / On Demand available after airing until 24 Jan, 2019.

Register free: http://www.chromatographyonline.com/lcgc_w/spectrometry
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