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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 |

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 |

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 |

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 |

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 |

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 |

Beyond Compliance and the FDA Unique Device Identification Rule - How to Achieve Global Standardization by LANSA

February 2014 - (Free Research)
This brief resource explores what the US Food and Drug Administration (FDA) Unique Device Identification (UDI) Rule is, why it was created, and how GS1 standards can be used to achieve compliance. Read on now to learn more. 
(WHITE PAPER) READ ABSTRACT |

HPC Storage: Taming the Data Torrent by Dell, Inc. and Intel®

August 2011 - (Free Research)
Check out this latest issue of HPC source to learn about the current state of high performance computing and what top experts predict for the coming decade. 
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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 |

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 |

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 |

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 |

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 |

UNDERSTANDING PCI MOBILE PAYMENT PROCESSING SECURITY GUIDELINES by Intel

September 2013 - (Free Research)
This expert guide from SearchSecurity.com discusses the new Payment Card Industry (PCI) Mobile Payment Acceptance Security Guidelines and examines how to ensure compliance in a world where mobile payment has become ingrained into everyday life. 
(EGUIDE) 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 |

Presentation Transcript: Go Forth & Comply - New Virtualization Guidelines from the PCI Council by Dell SecureWorks UK

August 2011 - (Free Research)
In this presentation transcript, principal security consultant at Dell SecureWorks, discuss the issues confronting organizations who wish to use virtualization technologies with their Cardholder Data Environment, summarize and clarify the recommendations from the PCI council and more. 
(PRESENTATION TRANSCRIPT) READ ABSTRACT |

The Critical Security Controls – Moving Beyond the Checklist Mentality by Lumension

August 2009 - (Free Research)
The "Critical Security Controls" (CSC) guidelines are designed to help organizations move beyond a "checklist" mentality by making security an integral part of, instead of an adjunct to, the operations and management of systems and networks. Learn more about the CSC guidelines and how they can help your organization. 
(PODCAST) 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 |

Vulnerability Management for GLBA Compliance by Qualys, Inc.

May 2008 - (Free Research)
The QualysGuard vulnerability management and policy compliance solution helps financial institutions to meet many key security guidelines. 
(WHITE PAPER) READ ABSTRACT |

Setting standards in IT Industries by DLT Solutions

March 2012 - (Free Research)
Building and adhering to security standards are essential for mitigating risk and ensuring adequate IT security. NIST is one of the first risk assessment standards, offering guidelines for securing the IT infrastructure. In this e-guide, gain an in-depth look into NIST and uncover how to decrease the risks that your industry faces. 
(EGUIDE) READ ABSTRACT |

SearchCompliance.com E-guide: A lesson in database security: What every compliance officer needs to know by IBM

August 2011 - (Free Research)
Too many enterprise databases are leaking sensitive information. Yet the solution to these problems is simple: user education, coupled with a new breed of database activity monitoring tools. This e-guide provides guidelines for establishing a data protection framework and teaching the right way to handle data. 
(EGUIDE) READ ABSTRACT |

How Automated Solutions Can Help with Efforts Toward Sarbanes-Oxley Compliance by Varonis

September 2008 - (Free Research)
This document provides a brief overview of the Sarbanes-Oxley Act, (Sections 302 and 404), the impact of SOX on IT Departments, and the Varonis Data Governance solution for critical portions of the Sarbanes-Oxley Act of 2002. 
(WHITE PAPER) READ ABSTRACT |

Leveraging a Maturity Model to Achieve “Proactive Compliance” by Symantec Corporation

August 2009 - (Free Research)
Read this paper to learn about a new approach to compliance that seeks to move beyond the short-term goal of passing an audit and to incorporate compliance into an organization's operations in a more proactive sense utilizing the Capability Maturity Model. 
(WHITE PAPER) READ ABSTRACT |

WagerWorks Takes Fraudsters Out of the Game Using iovation Device Reputation by iovation, Inc.

December 2009 - (Free Research)
In this paper WagerWorks covers how to deal with fraud challenges and resolution requirements of the casino industry. 
(CASE STUDY) READ ABSTRACT |

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