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Case Study from IDC: Speeding the Cure: Kalypsys Deploys Xerox DocuShare CPX to Accelerate Drug Development by Xerox DocuShare

May 2008 - (Free Research)
Learn how Kalypsis, a clinical stage pharmaceutical company, is leveraging Xerox DocuShare Enterprise Content Management to control content for regulatory operations and clinical trials. 
(CASE STUDY) READ ABSTRACT |

Implementing Breakthrough Technology for Clinical Development Modeling and Simulation by Univa UD

April 2008 - (Free Research)
When GlaxoSmithKline was challenged with improving efficiency in modeling and simulation, their clinical development research team turned to Univa technology for faster methods of establishing and running models for a drug’s effects on the body. 
(CASE STUDY) READ ABSTRACT |

Sage ERP X3 Helps Aceto Corporation Manage Complicated Compliance Regulations by Sage North America

October 2010 - (Free Research)
This case study explains how with Sage ERP X3, Aceto Corporation’s business processes are streamlined and automated. The company is finding it easier to comply with the financial reporting responsibilities placed on publicly-traded companies. Read on to learn how Aceto benefited from Sage ERP X3. 
(CASE STUDY) READ ABSTRACT |

Validation Process and Compliance Support with IBM Maximo Asset Management in Regulated Industries by IBM

December 2010 - (Free Research)
While there is no single method to guarantee software compliance, IBM Maximo® Asset Management can provide e-signature and e-record (audit trail) capabilities that support efforts to comply with regulations and guidelines related to e-records and e-signatures. 
(WHITE PAPER) READ ABSTRACT |

FlexNet and FDA 21 CFR Part 11 by Apriso Corporation

March 2011 - (Free Research)
Manufacturers regulated by the FDA 21 CFR Part 11 regulations understand that the integrity of manufacturing processes must be achieved and maintained in order to sustain compliance. The purpose of this document is to demonstrate that Apriso FlexNet platform and application suite can support the intent of the 21 CFR Part 11 regulatory guidelines. 
(WHITE PAPER) READ ABSTRACT |

ERP Software Acquisition in an FDA Regulated Environment by SoftBrands, Inc.

March 2008 - (Free Research)
This white paper presents a guideline to help you select an ERP system for your FDA validation. Explore a five phase software acquisition life cycle model to help you accomplish these objectives as efficiently as possible. 
(WHITE PAPER) READ ABSTRACT |

Adaptive Security for the Health/Pharma Vertical by Juniper Networks, Inc.

April 2011 - (Free Research)
Healthcare and pharmaceutical organizations are more sophisticated than ever before; but with that sophistication, they also face new challenges. 
(WHITE PAPER) READ ABSTRACT |

Managing Product Recalls to Reduce Risk and Minimize Cost by Sage North America

January 2009 - (Free Research)
With an integrated enterprise system like Sage ERP X3, food producers can use the same system to address industry-specific requirements and product recalls. 
(WHITE PAPER) READ ABSTRACT |

Pharmaceutical Services Company Accelerates Virtual Desktops by Cisco Systems, Inc.

July 2012 - (Free Research)
This case study demonstrates how Quintiles Pharmaceutical Services extended WAN optimization to 100 percent of their virtual desktop infrastructure and improved traffic flow with their existing bandwidth, allowing for secure and centralized data and access control, and high levels of employee satisfaction. 
(CASE STUDY) READ ABSTRACT |

Why Life Sciences need Integrated Information Governance more than Ever by RSD

February 2012 - (Free Research)
Across all industries, organizations are adopting information governance solutions to address challenges at the intersection of two trends: an explosion of content and the expansion of regulations and business requirements. This resource explores the nature of these challenges within the pharmaceutical industry. 
(WHITE PAPER) READ ABSTRACT |

Leading Pharmaceutical Company Reduces Costs to Meet CFR Compliance Through Digital Signature Implementation by Hexaware Technologies

October 2011 - (Free Research)
In this brief case study, discover eSignature's method of capturing electronic signatures at appropriate points in the work flows, storing relevant information, and enabling an audit trail to be retrieved for each applicable asset. 
(CASE STUDY) READ ABSTRACT |

Pharmaceutical Company Meets RTOs, RPOs and Regulatory Requirements with Veeam by Veeam Software

May 2014 - (Free Research)
Check out this case study involving pharmaceutical giant JGL and how they overcame their VM backup and replication challenges by implementing Veeam software. 
(CASE STUDY) READ ABSTRACT |

Making the Right Move to a Managed Service Provider for SSL VPN by MegaPath Inc.

March 2010 - (Free Research)
Adoption of SSL VPNs is growing rapidly. A sample of areas in which SSL VPNs can help include serving more communities, supporting more access environments, providing access without application and network changes, enforcing compliance, protecting the network, quickly modifying access policies, and ensuring business continuity. 
(WHITE PAPER) READ ABSTRACT |

The Total Economic Impact™ of Oracle Enterprise Manager Configuration Management Pack, and Provisioning and Patch Automation Pack by Oracle Corporation

March 2009 - (Free Research)
Learn how Oracle's comprehensive industry leading configuration management and provisioning automation solutions help you reduce application management costs while delivering greater control and compliance. 
(WHITE PAPER) READ ABSTRACT |

CW+: Analyst's take: Benefits of Siemens product lifecycle management software for life sciences by ComputerWeekly.com

January 2011 - (Free Research)
Siemens product lifecycle management (PLM) Software for life sciences can help medical device manufacturers manage compliance requirements while supporting greater collaboration, ultimately reducing costs while improving patient outcomes. 
(WHITE PAPER) READ ABSTRACT |

A New Approach to Verifying and Validating Medical Device Development by IBM

December 2010 - (Free Research)
The list of features in medical devices is rapidly rising: Even the simplest of medical devices house more and more system components, which add greater functionality to the device at a low cost. But by adding components, device software becomes complex and burdens compliance testing and premarket certification activities. 
(WHITE PAPER) READ ABSTRACT |

Pervasive Data Profiler v4 by Pervasive Integration

January 2008 - (Free Research)
Pervasive Data Profiler™ ensures data quality. Proactively audit all types of data; automate testing against changing business data quality needs and compliance regulations. Get hyper-fast, multithreaded processing of large data sets or sample data 
(WHITE PAPER) READ ABSTRACT |

Real-time Monitoring, Alerts, and Analysis Offer In-Depth Security by Dell SecureWorks UK

March 2012 - (Free Research)
In this case study explore how implementing Dell SecureWorks enabled Pharmaceutical firm, ProStrakan, to enhance its security and compliance posture by providing 24/7 monitoring, instant alerts and in-depth threat analysis. 
(CASE STUDY) READ ABSTRACT |

Making Office 365 More Secure and Compliant by Proofpoint, Inc.

December 2011 - (Free Research)
Microsoft has done a good job at developing a robust and scalable platform in Office 365, but there are some organizations that will need compliance and security capabilities not natively available. View this paper to explore what Office 365 will and will not do and where supplemental offerings from third party vendors will prove to be beneficial. 
(WHITE PAPER) READ ABSTRACT |

Tips on Implementing Database Auditing to Address Security & Compliance Requirements  by IBM

December 2010 - (Free Research)
Implementing Database Security and Auditing (Elsevier Digital Press) is the definitive guide for information security professionals, DBAs and auditors. You can now download Chapter 12, “Auditing Categories”.  In this chapter, you’ll learn which audit logging trails you need to address key security and compliance requirements. 
(BOOK) READ ABSTRACT |

Choosing the Right Enterprise Resource Planning (ERP) System: How to Avoid the 7 Fatal Flaws by CDC Software - Ross Enterprise

November 2008 - (Free Research)
This paper explains the importance of choosing the Right Enterprise Resource Planning (ERP) System to avoid the 7 Fatal Flaws. 
(WHITE PAPER) READ ABSTRACT |

AMAG Pharmaceuticals by Virtual Computer, Inc.

January 2011 - (Free Research)
Discover how AMAG Pharmaceuticals achieved 56% in external desktop support savings and met their mobility needs while avoiding costly infrastructure investments with Intelligent Desktop Virtualization (IDV). Read this case study to find out why AMAG chose IDV instead of traditional server-hosted VDI. 
(WHITE PAPER) READ ABSTRACT |

eBook - Email Archiving: Planning, Policies and Product Selection - Chapter 1: Email-Archiving Project Roadmap by SearchExchange.com

June 2009 - (Free Research)
Get the fundamentals of email archiving from start to finish in this e-book, “Email Archiving: Planning, policies and product selection.” Each chapter of this e-book will guide IT managers through the individual phases of the email-archiving project process. 
(EBOOK) READ ABSTRACT |

Lower your IT Costs with Oracle Database 11g Release 2 by Oracle Corporation

October 2011 - (Free Research)
This white paper contains a sampling of real business results that organizations around the world, in a variety of industries, have achieved by upgrading and standardizing on Oracle Database 11g. 
(WHITE PAPER) READ ABSTRACT |

Digital Trust in the Cloud: Liquid Security in Cloudy Places by CSC

November 2011 - (Free Research)
While some individual users are experimenting with cloud processing, other users have already fully committed to the cloud as an important part of their enterprise architecture and operation. Read this white paper to learn about the evolution of cloud processing and whether or not the cloud processing boom will continue. 
(WHITE PAPER) READ ABSTRACT |

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