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Documents related to » drug therapy


Mutual Drug Selects Epicor TDX » The TEC Blog
Mutual Drug Selects Epicor TDX » The TEC Blog TEC Blog     TEC Home     About TEC     Contact Us     About the Bloggers     Follow TEC on Twitter    RSS   Discussing Enterprise Software and Selection --> Fast, Accurate Software Evaluations TEC helps enterprises evaluate and select software solutions that meet their exacting needs by empowering purchasers with the tools, research, and expertise to make an ideal decision. Your software selection starts here. Learn more about TEC s

DRUG THERAPY: activant, edi, Epicor, epicor 9, epicor erp, epicor tdx, ERP, industry watch, value added network, van, TEC, Technology Evaluation, Technology Evaluation Centers, Technology Evaluation Centers Inc., blog, analyst, enterprise software, decision support.
12-02-2013

Automotive Industry and Food, Safety, and Drug Regulations
Enterprise application providers wanting to address the distinct regulatory requirements of the automotive, food, safety, and life sciences industries need to offer enterprises industry-oriented enterprise resource planning systems that are sound and compliance-ready.

DRUG THERAPY: and Food, Safety, and Drug Regulations Automotive Industry and Food, Safety, and Drug Regulations P.J. Jakovljevic - March 2, 2007 Read Comments Automotive Industry Treading on Regulations The issues of quality and safety in the automotive industry have recently become about more than simply complying with such regulatory requirements as the Automotive Right-to-Repair bill. Rather, for companies in the automotive industry, these issues are about maintaining consumer confidence, making certain companies
3/2/2007

Drug Pedigree Guidelines and How Software Can Help
Drug manufacturers and retailers are tightening their data collection and reporting processes to meet new US Food and Drug Administration (USFDA) guidelines. But which software offerings are best placed to help drug manufacturers comply with the new guidelines?

DRUG THERAPY: Drug Pedigree Guidelines and How Software Can Help Drug Pedigree Guidelines and How Software Can Help Ashish Labh and Joseph J. Strub - July 11, 2008 Read Comments This is a modified version of the article originally published July 19, 2006. Counterfeit and adulterated drugs are an increasing problem, particularly in the United States. Not only do these activities strip profits from legitimate drug manufacturers, but they can also pose a health risk to the consumer. As a result, the US Food and Drug
7/11/2008

Cigna Finds Good Therapy: Building a More Efficient Risk Management, Compliance, and System Security Program
As a provider of employee benefits, CIGNA must observe a bevy of regulatory compliance mandates. Because much of its efforts are compliance-focused, it continually embraces technology, searching for new products to better manage its benefit offerings and track its security risks. With QualysGuard’s vulnerability management solution, CIGNA has mitigated vulnerabilities and remained up-to-date with compliance regulations.

DRUG THERAPY:
10/31/2007 11:08:00 AM

Thou Shalt Manage (and Cherish) Thy (Best) Suppliers
Read this in-depth report from TEC Analyst P.J. Jakovljevic to find out why supplier management is crucial. In its recent report, Shifting C-level Business Priorities as the Recovery Takes Hold, Saugatuck Technologies claims that top business priorities are returning to a pattern more consistent with a growth economy. Read this in-depth report from TEC Analyst P.J. Jakovljevic to find out why supplier management is crucial.

DRUG THERAPY: new US Food and Drug Administration (FDA) regulation that sternly says “take the drug XYZ off the market… it is not safe!” The manufacturer in this case has to quickly find all relevant contracts, amend them, present them for a review to proper instances, and execute new contracts in its trading network. The mass contract creation ability and the ability to respond to large-scale contract changes in one fell swoop (from contract search results) are essential here to ensure compliance of all
11/12/2010 1:41:00 PM

HCIMS - Clinical Information System RFP Template


DRUG THERAPY: HCIMS - Clinical Information System RFP Template covers industry-standard functional criteria of HCIMS - Clinical Information System that can help you easily gather and prioritize your business needs in a simple and categorized excel document. More than a RFP template, it is a working document that serves as a knowledge base reference throughout the life-span of your HCIMS - Clinical Information System software project. Includes: ADT (admission, discharge, and transfer), Global Requirements, Patient Information, Orders, Plan of Care, Work Plan, Kardex and Summary, Flow Sheets and Vitals, MAR and Medications, Critical Care, L&D Fetal Monitoring, Clinical Record, Reference and Reports, HIPAA (Health Insurance Portability and Accountability Act), Interfaces, Ease of Use, Technical and Support, and Product Technology






Case Study: Securing Servers, Oracle Databases, and Embedded Systems in a Health Care Environment
A non-profit hospital needed to protect its critical clinical systems without either interrupting system availability or overloading the small IT security team. The hospital had to overcome several vulnerabilities, such as the fact that some clinical systems could not be patched due to Food and Drug Administration (FDA) regulations. Find out how a server security solution helped the hospital address these challenges.

DRUG THERAPY: due to Food and Drug Administration (FDA) regulations. Find out how a server security solution helped the hospital address these challenges. Case Study: Securing Servers, Oracle Databases, and Embedded Systems in a Health Care Environment style= border-width:0px; />   comments powered by Disqus Related Topics:   Security,   Firewall,   Intrusion Detection,   Network Security Monitoring,   Site Management,   Server,   IT Monitoring and Management,   Network Monitoring Source: Blue Lane
5/1/2008 12:29:00 PM

Ross Systems Focus Yields More Value For Process Manufacturers
For a vendor, focus is good, as it often results with more value to its targeted customers. A highly focused vendor can also remain profitable even in difficult economic times. One example of a vendor delivering more by covering less is Ross Systems.

DRUG THERAPY: sciences, and food & drug administration (FDA) safety functions for the food and beverage industries. With such a deep industry knowledge, understanding the company s flagship product, iRenaissance , means understanding not only what its customers do, but also how they do it. The mid-market focus also leads Ross to a technology strategy that allows customers to tailor-fit systems to their current needs through incremental deployments. Customers can add product modules, or expand their implementation
4/10/2002

Medical Device Manufacturers Can Leverage ERP/CRM Software to Facilitate FDA Compliance
Medical Device Manufacturers Can Leverage ERP/CRM Software to Facilitate FDA Compliance. Find Free Device and Other Solutions to Define Your Project In Relation To FDA Compliance and ERP/CRM Software. The US Food and Drug Administration (FDA) requires pharmaceuticals and medical device companies to comply with numerous standards. Medical device manufacturers have long embraced enterprise resource planning (ERP) and customer relationship management (CRM), but primarily use them to achieve operational efficiencies. However these systems can play a significant role in their abilities to comply with strictly FDA regulations.

DRUG THERAPY: The US Food and Drug Administration (FDA) requires pharmaceuticals and medical device companies to comply with numerous standards. Medical device manufacturers have long embraced enterprise resource planning (ERP) and customer relationship management (CRM), but primarily use them to achieve operational efficiencies. However these systems can play a significant role in their abilities to comply with strictly FDA regulations. Medical Device Manufacturers Can Leverage ERP/CRM Software to Facilitate FDA
3/14/2006 10:41:00 AM

The Name and Ownership Change Roulette Wheel for Marcam Stops at SSA GlobalPart Two: Marketing By Invensys
IPS was hoping that the early product vision and venerable reputation that Marcam has in the process manufacturing market for providing plant-centric ERP solutions might finally play well to capturing the marketing opportunity.

DRUG THERAPY: the US Food and Drug Administration (FDA) and the World Health Organization (WHO) would soon extend into the food and beverage industries. Therefore, in 2003, IPS was to focus on the plant management needs of food and beverages, life sciences, and specialty chemical industries, since many pre-Y2K regulated process manufacturing companies have invested heavily in ERP systems, with the aim of running their businesses using a single, integrated application from top to bottom. However, a great part of them
10/15/2004

Market Insight: Strategies for Overcoming Compliance Issues in the Pharmaceutical Industry
Strategies for Overcoming Compliancy Issues in the Pharmaceutical Industry: a recipe for success. To successfully meet compliance demands, pharmaceutical manufacturers must develop, implement, and track the effectiveness of a company-wide compliance strategy. Key to that strategy is to adopt industry-specific enterprise software with functionality that supports Federal Drug Administration (FDA) requirements. Learn more about the criteria and recommendations you need to achieve compliance in the pharmaceutical industry.

DRUG THERAPY: functionality that supports Federal Drug Administration (FDA) requirements. Learn more about the criteria and recommendations you need to achieve compliance in the pharmaceutical industry. Market Insight: Strategies for Overcoming Compliance Issues in the Pharmaceutical Industry style= border-width:0px; />   comments powered by Disqus Related Topics:   Enterprise Resource Planning (ERP),   Process Manufacturing,   Formula/Recipe,   Product Information Management (PIM),   Shipping and Receiving,
5/22/2009 4:00:00 PM


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