Information Technology
Research Library
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TranSenda International
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Leverage the Microsoft Office System to conduct clinical trials like never before - now each person can have their own view of all the latest information in a controlled environment, combining your investment in applications and the knowledge of your staff.
The Microsoft Office system is comprised of the familar Microsoft Office applications. Microsoft Word, Excel, PowerPoint and Outlook are ...
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Lean & Mean Business Systems, Inc.
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Medical Device Manufacturers have always focused on bringing innovative high quality products to market. Yet shifting financial, regulatory and globalization landscapes call for closed-loop product management strategies that can keep up with the increasing innovation tempo and complexity of medical devices while at the same time, lower cost, increase quality, and facilitate compliance with ...
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Lancaster Laboratories
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Profiling of impurities in biopharmaceuticals and their associated intermediates and excipients is a regulatory expectation. Since residuals are typically present at low levels in difficult sample matrices, development and validation of assays can be quite challenging. Matrix types can vary greatly due to the fact that sampling at a variety of process steps is required to accurately monitor ...
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DZS Software Solutions
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The challenges facing our industry to effectively meet the clinical data study standards set out by the Clinical Data Interchange Standards Consortium (CDISC) specifically with regards to the Study Data Tabulation Module (SDTM) and the Analysis Data Model (ADaM) can be daunting. Our ADaM Data Conversion and Reporting Toolkit may be the solution you are looking for to generate all of your safety ...
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Rondaxe
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How to Guide for Writing a Drug Master File Introduction A drug master file (DMF) is a proprietary document typically written by or for the manufacturer to protect manufacturing information, an intermediate, starting raw material, Active Pharmaceutical Ingredient (API), description of production site/s or for other special requests. Most often, DMF's are written to protect the manufacturing ...
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