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Featured Whitepaper
Protect Your Scientific Intellectual Property: Proof of Lab Informatics Data Authenticity is Your Best Legal Defense
Sponsored By: Surety, LLC
As a pharmaceutical or bio-sciences firm, your research, formulas and clinical findings are the "lifeblood" of your business. But if you aren’t protecting the integrity of your research data in your lab management workflows, you risk losing ownership, revenue and potentially your business if you can't prove time of creation (“first-to-invent”) and authenticity. Learn how you can integrate simple, cost-effective and automated controls to protect your scientific intellectual property for the long term, and ease the costly, manual task scientists must follow to “sign and witness” volumes of research records. |
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Transparency Paradigm: selecting a CRO for the Endocrine Program
Author: Ronald C. Biever, Chief Scientific Officer
Sponsored By: Smithers Viscient
Application Note abstract: In 2009, the House Appropriations Committee report directed the EPA to publish a list of chemicals for screening in the Endocrine Disruptor Screening Program (EDSP) that includes drinking water contaminants such as pharmaceuticals and personal care products, and to issue orders for the testing of these chemicals. Given the new and unique challenges presented in the US EPA’s EDSP, you may need to reconsider your CRO selection process. The white paper, “The Transparency Paradigm: How to select the right CRO for your Endocrine Disruptor Screening Program needs”, offers practical advice that can help to increase the likelihood of successfully completing EDSP testing for your organization.
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Method Transfer of Loratadine from HPLC to UPLC using the ACQUITY UPLC H-Class System
Author: Peter Alden
Sponsored By: Waters Corporation
The compendial HPLC method for analysis of Loratadine is transferred to the quaternary-based ACQUITY UPLC H-Class System and migrated to UPLC. We illustrate that this new system is ideal for laboratories seeking improvements in efficiency and cost-effectiveness. |
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Simplifying Qualitative, Quantitative Analysis in Discovery DMPK
Author: Robert S. Plumb and Paul D. Rainville
Sponsored By: Waters Corporation
In this application note, we demonstrate the use UPLC/MS to perform both quantitative and qualitative analysis, providing high-quality MS, MRM, and MS/MS data for candidate drug molecules in discovery. Rapid data collection ensures that both MS and MS/MS peaks are well characterized and that high-quality spectra are acquired. |
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Bulk Inspection of Tablets: Assuring Product Quality at Manufacturing and Packaging
Sponsored By: SYMETIX
Achieve new levels of product quality and inspection efficiency in the manufacturing and packaging of tablets. Learn the pros and cons of manual inspection, mechanical sorting, blistering, single-file optical systems and a new class of automated bulk vision inspection systems. The latest technology ensures top-quality products while minimizing risk, increasing throughput and containing costs. |
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Assessing dry powder inhalers
Author: Mark Copley, Sales Director, Copley Scientific
Sponsored By: Copley Scientific Limited
The performance characterization of dry powder inhalers (DPI) recognizes the importance of three factors: the device, the formulation and the patient. Successful product development demands an understanding of how each of these shapes drug delivery, and how to test the product in a relevant way. |
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