Information Technology

Information Technology Research Library

Managing Clinical Trials Through the Microsoft Office System
TranSenda International
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 ...
 
Total Product Lifecycle Management: Lowering Costs while Increasing Quality
Lean & Mean Business Systems, Inc.
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 ...
 
Analytical Strategies for Monitoring Residual Impurities Encountered In Bioprocessing
Lancaster Laboratories
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 ...
 
Converting SDTM Data to ADaM Data and Creating Submission Ready Safety Tables and Listings
DZS Software Solutions
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 ...
 
DMF Preparation
Rondaxe
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 ...
 

Information Technology Video

NuViewHR Product Suite Demo NuView Systems See how a NuView’s HRIS can provide “strategic” help to your organization, from hiring to separation.
 
Enabling Business Strategy through Mobile HR Technology NuView Systems Learn how mobile HR technology enables you to review, revise and approve common human resource requests from anywhere via your mobile device.
 
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Information Technology Blue Grotto Technologies, Inc. Information
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