- How to Control Supersaturation
- Cookbook for Supersaturation
- Live Q&A with METTLER TOLEDO Expert
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- Method of Measurement pH
- Good Laboratory Practice pH with Automated Lab Reactors
- Automated and Controlled pH Dosing
- Live Q&A with METTLER TOLEDO Expert
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- What is a Polymorph?
- Why is it Important to Understand Polymorphs?
- How to Distinguish Polymorphs
- Example of Controlling a Crystallization for a Specific Product Form
- Live Q&A with METTLER TOLEDO Expert
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- Scale-up with Heat Flow Calorimetry
- iC Safety for Safe Processes
- Reaction Calorimetry with gold standard measurements in RC1
- Live Q&A with METTLER TOLEDO Expert
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Regulatory pressure is pushing pharmaceutical companies to make the move in quality control from paper to electronic records. This process requires a computer system validation (CSV), which can appear extremely complex and time consuming.
Exaggerated efforts to be compliant have been described by Bob McDowall, a renowned auditor, as "death by compliance".
This webinar guides you through the Computer System Validation process in line with regulatory requirements. This includes milestones, estimated implementation times as well as touching on possible pitfalls. Lastly, it will offer general recommendations for speedy and cost effective processes.
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Presenter Information: L. Craig Jones, Application Scientist, Agilent Technologies, Inc.
Craig has been with Agilent since 2004 as an ICP-MS applications scientist. He has been involved with multiple type of applications for ICP-MS, including environmental, pharmaceutical, nutraceutical, semiconductor, geologic, and clinical analyses, to name a few. Previous to Agilent He worked in an environmental lab performing analysis and supervising both the inorganic and organic sections of the laboratory. In his spare time, Craig enjoys volunteering at the local marine science center, mountain biking, hiking and relaxing at the beach. Craig obtained a bachelor of science degree in chemistry from Fort Lewis College in Durango, CO.
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- How to Extract Reaction Rates Efficiently
- How to Gain Mechanistic Insights into your Reaction Chemistry
- Live Q&A with METTLER TOLEDO Expert
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Presentations
Modeling & Feedback Control of Batch & Continuous Crystallization Systems
Professor Zoltan Nagy - Purdue University
Nucleation & Growth Kinetics for Combined Cooling & Antisolvent Crystallization in an MSMPR System - Estimating Solvent Dependency
Jennifer Moffitt Schall - Massachusetts Institute of Technology
Reactive Crystallization and Recrystallization for Energetic Material
Matthew Jorgensen - Nalas Engineering
During this live stream, a technology and application expert will be online to answer your questions live.
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Alissa Interpret is a USA Class I Exempt Medical Device, Europe CE IVD, Canada and Australia Class I IVD Device
- Expand your access to up-to-date clinical knowledge bases
- Unlock translocation/fusion genes in your assays
- Bring Whole Genome Sequencing closer to reality with combined NGS+CGH analysis
- Integrate your automated pipelines and LIMS with new open API options
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Angiotensin II receptor blocker (ARB) drug products are commonly used to treat high blood pressure and heart failure. Recently, it was found that some ARB drug products contained carcinogenic nitrosamine impurities; as a result, many such products have been recalled. As a result, there is a renewed interest in the development of route/easy to use LC/MS and LC/MS/MS analytical methods capable of detecting these problematic nitrosamine impurities at very low levels (e.g. ppb). The webinar will begin by discussing the critical aspects needed to properly setup the LC for this application, followed by discussion recent results obtained using both a QQQ mass spectrometer and a high resolution QTOF mass spectrometer. The webinar will contain a live demonstration of the use of Agilent’s MassHunter Quant-My-Way software to determine the limit of detection and limit of quantitation of the six nitrosamines listed by the USFDA, and also the simultaneous detection of 11 nitrosamine impurities.
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Handling Risks and Errors in Pharma Records - there should be procedures to stay compliant. With their focus on Data Integrity, regulation authorities are ever pushing the pharmaceutical industries towards electronic records. The number of FDA warning letters with citations of data integrity violations reveal that not every pharma company interprets the rules correctly and with an acceptable risk management policy.
Conservative practices might overlook the dynamic of regulations and might end in incompliance just because the interpretation of rules have evolved.
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Presenter Information: Dr. Sima Singha, ICP-OES Application Scientist, Atomic Spectroscopy, Agilent Technologies, Inc.
Sima has over fifteen years of hands on experience as an applications scientist in the field of atomic spectroscopy. Before joining Agilent in 2017, managed an agricultural chemistry laboratory for the analysis of water, soil, and plant tissue digests using ICP-OES for various EPA methods. She received a Ph.D. degree in Chemistry from the University of Illinois at Chicago with numerous peer-reviewed publications.
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